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Q35762932-B3E1D21B-6F2B-4431-A835-217B274336C6
Q35762932-B3E1D21B-6F2B-4431-A835-217B274336C6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35762932-B3E1D21B-6F2B-4431-A835-217B274336C6
Intrafamilial phenotypic variability in families with RDS mutations: exclusion of ROM1 as a genetic modifier for those with retinitis pigmentosa
P2860
Q35762932-B3E1D21B-6F2B-4431-A835-217B274336C6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35762932-B3E1D21B-6F2B-4431-A835-217B274336C6
rank
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type
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wasDerivedFrom
ff4f3b95f6f5616b236ded492af1886f119ecf7b
P2860
Autosomal dominant central areolar choroidal dystrophy and a novel Arg195Leu mutation in the peripherin/RDS gene.