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Q34657855-F7E9096B-664D-4854-934C-DC2C05A6D97A
Q34657855-F7E9096B-664D-4854-934C-DC2C05A6D97A
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Statement
http://www.wikidata.org/entity/statement/Q34657855-F7E9096B-664D-4854-934C-DC2C05A6D97A
Loss-of-function mutations in WDR73 are responsible for microcephaly and steroid-resistant nephrotic syndrome: Galloway-Mowat syndrome.
P2860
Q34657855-F7E9096B-664D-4854-934C-DC2C05A6D97A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34657855-F7E9096B-664D-4854-934C-DC2C05A6D97A
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wasDerivedFrom
8e97570a5447917871a8bb69712d8aaaff53fcbf
P2860
A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS