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Q34329671-32E083FD-ACA9-42AA-A97A-8A9D978A1B6A
Q34329671-32E083FD-ACA9-42AA-A97A-8A9D978A1B6A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34329671-32E083FD-ACA9-42AA-A97A-8A9D978A1B6A
A novel recessive GUCY2D mutation causing cone-rod dystrophy and not Leber's congenital amaurosis
P2860
Q34329671-32E083FD-ACA9-42AA-A97A-8A9D978A1B6A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34329671-32E083FD-ACA9-42AA-A97A-8A9D978A1B6A
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
04f72d1e4e4d5bc59961ff373dc0da8d616e3cea
P2860
Mutation analysis identifies GUCY2D as the major gene responsible for autosomal dominant progressive cone degeneration.