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Q21710708-3E5A137F-6716-49DA-BF6B-1CAB05799EE2
Q21710708-3E5A137F-6716-49DA-BF6B-1CAB05799EE2
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http://www.wikidata.org/entity/statement/Q21710708-3E5A137F-6716-49DA-BF6B-1CAB05799EE2
Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness
P1433
Q21710708-3E5A137F-6716-49DA-BF6B-1CAB05799EE2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q21710708-3E5A137F-6716-49DA-BF6B-1CAB05799EE2
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P1433
American Journal of Human Genetics