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Q30415926-9D50C650-ED8E-4EF2-9E84-B8701615DCD3
Q30415926-9D50C650-ED8E-4EF2-9E84-B8701615DCD3
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Statement
http://www.wikidata.org/entity/statement/Q30415926-9D50C650-ED8E-4EF2-9E84-B8701615DCD3
Whole-exome sequencing identifies OR2W3 mutation as a cause of autosomal dominant retinitis pigmentosa.
P2860
Q30415926-9D50C650-ED8E-4EF2-9E84-B8701615DCD3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30415926-9D50C650-ED8E-4EF2-9E84-B8701615DCD3
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wasDerivedFrom
037d8bac3eed725de9a9ddbc35921b063ff6b595
P2860
Evaluation of 172 candidate polymorphisms for association with oligozoospermia or azoospermia in a large cohort of men of European descent.