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Q37426932-F1FE3BB2-B6BB-44BD-9E26-7AD1BEDD9D43
Q37426932-F1FE3BB2-B6BB-44BD-9E26-7AD1BEDD9D43
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http://www.wikidata.org/entity/statement/Q37426932-F1FE3BB2-B6BB-44BD-9E26-7AD1BEDD9D43
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients
P2860
Q37426932-F1FE3BB2-B6BB-44BD-9E26-7AD1BEDD9D43
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37426932-F1FE3BB2-B6BB-44BD-9E26-7AD1BEDD9D43
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wasDerivedFrom
16e3a992288b8bec9eabf5d8db6e113d1c75ce31
P2860
The contribution of GPR98 and DFNB31 genes to a Spanish Usher syndrome type 2 cohort.