Matches in Nanopublications for { ?s ?p "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP221080.RA-Xa-cizMzHiq6BMMziP03j-Z2R2zWojCgCmkDh9wBHU130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221080.RA-Xa-cizMzHiq6BMMziP03j-Z2R2zWojCgCmkDh9wBHU130_provenance.
- NP736.RADeclIYnrO7y71Fo2dG9qLT6PhvCcuvYfxlA6QVEixCg130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP736.RADeclIYnrO7y71Fo2dG9qLT6PhvCcuvYfxlA6QVEixCg130_provenance.
- assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP10007.RAP5A6-YSkl6aM1vi3KMcLiJEK_669MtK4xGGMhNiXaoA130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP10007.RAP5A6-YSkl6aM1vi3KMcLiJEK_669MtK4xGGMhNiXaoA130_provenance.
- NP237724.RAURvdD6ZamKXQ8Rwy0W5uXip01RJFBOB1kV4rYy7zjAo130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237724.RAURvdD6ZamKXQ8Rwy0W5uXip01RJFBOB1kV4rYy7zjAo130_provenance.
- NP237777.RAdYeF5q1BbnCqfxGEDLtDjy1A6tQ-tuuoEnUy-Jhgmz8130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237777.RAdYeF5q1BbnCqfxGEDLtDjy1A6tQ-tuuoEnUy-Jhgmz8130_provenance.
- assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP796159.RA6GsNiqSdruCW33BJNtLUOPnh1JpeCm3MQlbgdF-GX8g130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP796159.RA6GsNiqSdruCW33BJNtLUOPnh1JpeCm3MQlbgdF-GX8g130_provenance.
- NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_provenance.
- NP5080.RAR4VA4_S-3q6K97Razg9gzDi8PF5DYkoN6BXB1Z1oB38130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5080.RAR4VA4_S-3q6K97Razg9gzDi8PF5DYkoN6BXB1Z1oB38130_provenance.
- NP357125.RAkDm6f9606NvLHN8f-5mqpxK0RThMzm2FDuYDRjvsr5g130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357125.RAkDm6f9606NvLHN8f-5mqpxK0RThMzm2FDuYDRjvsr5g130_provenance.
- NP623591.RAYqH4JmEi1HCwb59XxqiVvk1FT-ueE88juIqA9cCrt20130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623591.RAYqH4JmEi1HCwb59XxqiVvk1FT-ueE88juIqA9cCrt20130_provenance.
- NP623593.RAfjkTFf0J40CdbWSk9sx_4cnMcO9hXH1o1xlZmTZtDAU130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623593.RAfjkTFf0J40CdbWSk9sx_4cnMcO9hXH1o1xlZmTZtDAU130_provenance.
- NP623596.RAZ3-1zIP5kCx_DiyvLf_vfYq6ZG_EvG9KxkxnTjsOt0c130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623596.RAZ3-1zIP5kCx_DiyvLf_vfYq6ZG_EvG9KxkxnTjsOt0c130_provenance.
- NP237810.RArQbmIXbYde3DggKSZw1ZPtix3-xPiEhMpeMxjc4tvuA130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237810.RArQbmIXbYde3DggKSZw1ZPtix3-xPiEhMpeMxjc4tvuA130_provenance.
- NP237715.RAAqNZ2b9-mMkZK9d0x3JgqM5LukMyB7YdbDz2H6JMhI4130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237715.RAAqNZ2b9-mMkZK9d0x3JgqM5LukMyB7YdbDz2H6JMhI4130_provenance.
- NP20321.RADRhHkoa6wjor_ZnVLulseVpabhs6Zi4rF-_NsN_7nG0130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20321.RADRhHkoa6wjor_ZnVLulseVpabhs6Zi4rF-_NsN_7nG0130_provenance.
- NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_provenance.
- NP623594.RAhEXrrfROTNb1Qqa237mvf6zsEPAjDS5dyK6nAZoPAZg130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623594.RAhEXrrfROTNb1Qqa237mvf6zsEPAjDS5dyK6nAZoPAZg130_provenance.
- NP623595.RArvTLAi0UMo_ijto9lVC89zc_l2C5CiicoULSAj-nRpA130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623595.RArvTLAi0UMo_ijto9lVC89zc_l2C5CiicoULSAj-nRpA130_provenance.
- NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_provenance.