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Q34051594-F1EACA44-1B61-4004-AF22-33E76B7CFBCC
Q34051594-F1EACA44-1B61-4004-AF22-33E76B7CFBCC
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http://www.wikidata.org/entity/statement/Q34051594-F1EACA44-1B61-4004-AF22-33E76B7CFBCC
Channelopathies: ion channel defects linked to heritable clinical disorders.
P2860
Q34051594-F1EACA44-1B61-4004-AF22-33E76B7CFBCC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34051594-F1EACA44-1B61-4004-AF22-33E76B7CFBCC
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wasDerivedFrom
f870ac80be09f42f1331bda0a0a18d0adcdbaf4e
P2860
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness