Matches in Nanopublications for { ?s ?p "[Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP674518.RAwpqFQJMH9zJlpPH1h2a7jEhTDkZLv4wEt6QHAcy0s5c130_assertion description "[Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674518.RAwpqFQJMH9zJlpPH1h2a7jEhTDkZLv4wEt6QHAcy0s5c130_provenance.
- NP1049082.RAQ8UAaB87LQb5sTPsfVQPudZTX01NmT6OQOWYb9KNXuA130_assertion description "[Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1049082.RAQ8UAaB87LQb5sTPsfVQPudZTX01NmT6OQOWYb9KNXuA130_provenance.
- assertion description "[Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.