Matches in Nanopublications for { ?s ?p "[We determined the fraction of families in a well-characterized cohort with a provisional diagnosis of autosomal dominant retinitis pigmentosa (adRP) that have disease-causing mutations in the X-linked retinitis pigmentosa GTPase regulator (RPGR) gene or the retinitis pigmentosa 2 (RP2) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP465622.RAtzw5iOWgj5Jkm_dEFvM0Cwsgl0UG3rFqSuMR_KSkCZg130_assertion description "[We determined the fraction of families in a well-characterized cohort with a provisional diagnosis of autosomal dominant retinitis pigmentosa (adRP) that have disease-causing mutations in the X-linked retinitis pigmentosa GTPase regulator (RPGR) gene or the retinitis pigmentosa 2 (RP2) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465622.RAtzw5iOWgj5Jkm_dEFvM0Cwsgl0UG3rFqSuMR_KSkCZg130_provenance.
- NP1049083.RABPUjeRBifZIUjLL7P-1p-c2kIcpwNbyExdZZUXjDf2w130_assertion description "[We determined the fraction of families in a well-characterized cohort with a provisional diagnosis of autosomal dominant retinitis pigmentosa (adRP) that have disease-causing mutations in the X-linked retinitis pigmentosa GTPase regulator (RPGR) gene or the retinitis pigmentosa 2 (RP2) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1049083.RABPUjeRBifZIUjLL7P-1p-c2kIcpwNbyExdZZUXjDf2w130_provenance.
- NP988544.RAymO0cWefa8BpzO0zawChfo5IjJnb5IdaAWW7msqJIgo130_assertion description "[We determined the fraction of families in a well-characterized cohort with a provisional diagnosis of autosomal dominant retinitis pigmentosa (adRP) that have disease-causing mutations in the X-linked retinitis pigmentosa GTPase regulator (RPGR) gene or the retinitis pigmentosa 2 (RP2) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988544.RAymO0cWefa8BpzO0zawChfo5IjJnb5IdaAWW7msqJIgo130_provenance.
- NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_assertion description "[We determined the fraction of families in a well-characterized cohort with a provisional diagnosis of autosomal dominant retinitis pigmentosa (adRP) that have disease-causing mutations in the X-linked retinitis pigmentosa GTPase regulator (RPGR) gene or the retinitis pigmentosa 2 (RP2) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_provenance.
- NP1049081.RAfC9L4rE2HOclXJ7ndnDG194SklPnEtQKkSdhrIBcTtc130_assertion description "[We determined the fraction of families in a well-characterized cohort with a provisional diagnosis of autosomal dominant retinitis pigmentosa (adRP) that have disease-causing mutations in the X-linked retinitis pigmentosa GTPase regulator (RPGR) gene or the retinitis pigmentosa 2 (RP2) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1049081.RAfC9L4rE2HOclXJ7ndnDG194SklPnEtQKkSdhrIBcTtc130_provenance.
- NP990936.RAnjBOiAttggX_g2Ml2HKu2doC7CUqk8IvY4ZgElF9YMI130_assertion description "[We determined the fraction of families in a well-characterized cohort with a provisional diagnosis of autosomal dominant retinitis pigmentosa (adRP) that have disease-causing mutations in the X-linked retinitis pigmentosa GTPase regulator (RPGR) gene or the retinitis pigmentosa 2 (RP2) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990936.RAnjBOiAttggX_g2Ml2HKu2doC7CUqk8IvY4ZgElF9YMI130_provenance.
- NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_assertion description "[We determined the fraction of families in a well-characterized cohort with a provisional diagnosis of autosomal dominant retinitis pigmentosa (adRP) that have disease-causing mutations in the X-linked retinitis pigmentosa GTPase regulator (RPGR) gene or the retinitis pigmentosa 2 (RP2) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_provenance.