Matches in Nanopublications for { ?s ?p "[The affected members of the Surinamese family have a severe early-onset form of autosomal recessive retinitis pigmentosa, which is caused by compound heterozygous mutations in the TULP1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP122262.RAwhIQODfPoozAXETv1hqYMzzxP1Axf9gDdxuvmnAVbUg130_assertion description "[The affected members of the Surinamese family have a severe early-onset form of autosomal recessive retinitis pigmentosa, which is caused by compound heterozygous mutations in the TULP1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122262.RAwhIQODfPoozAXETv1hqYMzzxP1Axf9gDdxuvmnAVbUg130_provenance.
- assertion description "[The affected members of the Surinamese family have a severe early-onset form of autosomal recessive retinitis pigmentosa, which is caused by compound heterozygous mutations in the TULP1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP227039.RAcXnTG0yS_q5HHphEuot3Xx-zt6ICF_dYV8k4IjY9B4U130_assertion description "[The affected members of the Surinamese family have a severe early-onset form of autosomal recessive retinitis pigmentosa, which is caused by compound heterozygous mutations in the TULP1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227039.RAcXnTG0yS_q5HHphEuot3Xx-zt6ICF_dYV8k4IjY9B4U130_provenance.
- NP185450.RA2sPfsD3Xlw7GKruc7VERCbkxs72oiO9NxqcZSFiZ1PA130_assertion description "[The affected members of the Surinamese family have a severe early-onset form of autosomal recessive retinitis pigmentosa, which is caused by compound heterozygous mutations in the TULP1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185450.RA2sPfsD3Xlw7GKruc7VERCbkxs72oiO9NxqcZSFiZ1PA130_provenance.