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Q37365488-A473E3F9-11E1-406C-87F8-FC7BAEB1B592
Q37365488-A473E3F9-11E1-406C-87F8-FC7BAEB1B592
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37365488-A473E3F9-11E1-406C-87F8-FC7BAEB1B592
A single-base substitution within an intronic repetitive element causes dominant retinitis pigmentosa with reduced penetrance
P2860
Q37365488-A473E3F9-11E1-406C-87F8-FC7BAEB1B592
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37365488-A473E3F9-11E1-406C-87F8-FC7BAEB1B592
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wasDerivedFrom
0d64f3ee24bd944817678ac32018cba23e1227c7
P2860
Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19