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Q30440790-B761AEE1-F7E9-40F7-9006-EBA251F343B9
Q30440790-B761AEE1-F7E9-40F7-9006-EBA251F343B9
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http://www.wikidata.org/entity/statement/Q30440790-B761AEE1-F7E9-40F7-9006-EBA251F343B9
Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families
P2860
Q30440790-B761AEE1-F7E9-40F7-9006-EBA251F343B9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30440790-B761AEE1-F7E9-40F7-9006-EBA251F343B9
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5a5ae1233d5f38d7bdb0b125cfe24dcaf7190c40
P2860
Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and clinical features associated with the most common mutation, Asp226Asn.