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Q35880740-0B5C7C0C-E75A-4DD8-929D-DAB32E740A2C
Q35880740-0B5C7C0C-E75A-4DD8-929D-DAB32E740A2C
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http://www.wikidata.org/entity/statement/Q35880740-0B5C7C0C-E75A-4DD8-929D-DAB32E740A2C
Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73.
P2860
Q35880740-0B5C7C0C-E75A-4DD8-929D-DAB32E740A2C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35880740-0B5C7C0C-E75A-4DD8-929D-DAB32E740A2C
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wasDerivedFrom
b4a1f15a25682c8b49ba003038d6f2a946ee4008
P2860
Loss-of-function mutations in WDR73 are responsible for microcephaly and steroid-resistant nephrotic syndrome: Galloway-Mowat syndrome.