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Q28237273-2A0463AA-FDAA-4211-B492-0623A814BE3C
Q28237273-2A0463AA-FDAA-4211-B492-0623A814BE3C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28237273-2A0463AA-FDAA-4211-B492-0623A814BE3C
A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46,XY patient with Denys-Drash syndrome
P2860
Q28237273-2A0463AA-FDAA-4211-B492-0623A814BE3C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28237273-2A0463AA-FDAA-4211-B492-0623A814BE3C
rank
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Statement
wasDerivedFrom
631cfb60b6d6cff201e2fb589c71eaa1a94abd19
P2860
Donor splice-site mutations in WT1 are responsible for Frasier syndrome.