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Q24294725-A9D49401-97E9-4379-B3E6-2069AC65B47A
Q24294725-A9D49401-97E9-4379-B3E6-2069AC65B47A
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Statement
http://www.wikidata.org/entity/statement/Q24294725-A9D49401-97E9-4379-B3E6-2069AC65B47A
Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa
P2860
Q24294725-A9D49401-97E9-4379-B3E6-2069AC65B47A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24294725-A9D49401-97E9-4379-B3E6-2069AC65B47A
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Statement
wasDerivedFrom
4dcd4caef8fed231d75c30b29c0f2bb6a84ba46d
P2860
A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration