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Q37363942-482234DE-0FBD-4741-A06E-CF509DED7EFC
Q37363942-482234DE-0FBD-4741-A06E-CF509DED7EFC
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http://www.wikidata.org/entity/statement/Q37363942-482234DE-0FBD-4741-A06E-CF509DED7EFC
Two novel PRP31 premessenger ribonucleic acid processing factor 31 homolog mutations including a complex insertion-deletion identified in Chinese families with retinitis pigmentosa.
P2860
Q37363942-482234DE-0FBD-4741-A06E-CF509DED7EFC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37363942-482234DE-0FBD-4741-A06E-CF509DED7EFC
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wasDerivedFrom
a55d6eea3d44bd12253d02fedac4b5f5e13430bd
P2860
Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families