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Q37323334-08F11244-21A3-46DA-B374-0BC1A993D0FE
Q37323334-08F11244-21A3-46DA-B374-0BC1A993D0FE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37323334-08F11244-21A3-46DA-B374-0BC1A993D0FE
Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.
P2860
Q37323334-08F11244-21A3-46DA-B374-0BC1A993D0FE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37323334-08F11244-21A3-46DA-B374-0BC1A993D0FE
rank
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type
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Statement
wasDerivedFrom
27438758100467c9b2b4cf78930c971e2df89258
P2860
Negative electroretinograms in retinitis pigmentosa.