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Q24307529-1775B89A-937F-4362-A131-BACC8DD368C0
Q24307529-1775B89A-937F-4362-A131-BACC8DD368C0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24307529-1775B89A-937F-4362-A131-BACC8DD368C0
RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophy
P1433
Q24307529-1775B89A-937F-4362-A131-BACC8DD368C0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24307529-1775B89A-937F-4362-A131-BACC8DD368C0
rank
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type
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Statement
P1433
Human Mutation