Matches in Nanopublications for { ?s ?p "[Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP35376.RAbiM6rXmrz3KZh_aCQ44cdhnfaTz5jDLN6hnWZeibX2U130_assertion description "[Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP35376.RAbiM6rXmrz3KZh_aCQ44cdhnfaTz5jDLN6hnWZeibX2U130_provenance.
- assertion description "[Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP35377.RANA7TK0ntEfrTtPCGVDgxZDpJiXyjNO6FhO4mC-veUwY130_assertion description "[Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP35377.RANA7TK0ntEfrTtPCGVDgxZDpJiXyjNO6FhO4mC-veUwY130_provenance.
- NP1276307.RA3OKL4_99LJ7qdTsYbA_YrjnEo2KT1BfLeoBkAqzWn2w130_assertion description "[Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1276307.RA3OKL4_99LJ7qdTsYbA_YrjnEo2KT1BfLeoBkAqzWn2w130_provenance.