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Q34281553-27F89521-F84B-465C-9FDD-8B2981B5EF07
Q34281553-27F89521-F84B-465C-9FDD-8B2981B5EF07
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Statement
http://www.wikidata.org/entity/statement/Q34281553-27F89521-F84B-465C-9FDD-8B2981B5EF07
Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations
P2860
Q34281553-27F89521-F84B-465C-9FDD-8B2981B5EF07
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34281553-27F89521-F84B-465C-9FDD-8B2981B5EF07
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wasDerivedFrom
41785f568b47292e3061d1ccd6e2734cbc26a4a1
P2860
An unusual phenotype of Frasier syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis.