Matches in Nanopublications for { ?s ?p "[A primary role of the ABCA4 gene in STGD1/FFM and AR CRD, together with the gene's involvement in an as-yet-unknown proportion of cases with AR RP, strengthens the idea that mutations in the ABCA4 gene could be the most frequent cause of inherited retinal dystrophy in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[A primary role of the ABCA4 gene in STGD1/FFM and AR CRD, together with the gene's involvement in an as-yet-unknown proportion of cases with AR RP, strengthens the idea that mutations in the ABCA4 gene could be the most frequent cause of inherited retinal dystrophy in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP237357.RAGMtynsJZ8JqdfeS8wW_jucMeLLSFEB2dVU-Z3_8WPSg130_assertion description "[A primary role of the ABCA4 gene in STGD1/FFM and AR CRD, together with the gene's involvement in an as-yet-unknown proportion of cases with AR RP, strengthens the idea that mutations in the ABCA4 gene could be the most frequent cause of inherited retinal dystrophy in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237357.RAGMtynsJZ8JqdfeS8wW_jucMeLLSFEB2dVU-Z3_8WPSg130_provenance.
- NP980.RAqeQs6Vn55NzdfstDKA6gUrT5TQPVv-8HarCdQxz5xns130_assertion description "[A primary role of the ABCA4 gene in STGD1/FFM and AR CRD, together with the gene's involvement in an as-yet-unknown proportion of cases with AR RP, strengthens the idea that mutations in the ABCA4 gene could be the most frequent cause of inherited retinal dystrophy in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP980.RAqeQs6Vn55NzdfstDKA6gUrT5TQPVv-8HarCdQxz5xns130_provenance.
- NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_assertion description "[A primary role of the ABCA4 gene in STGD1/FFM and AR CRD, together with the gene's involvement in an as-yet-unknown proportion of cases with AR RP, strengthens the idea that mutations in the ABCA4 gene could be the most frequent cause of inherited retinal dystrophy in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP293151.RAndVex_b5HWGcRQ7YSjNIF3ajqGV0h1iPrC0JSJyId7M130_provenance.