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A novel WT1 missense mutation presenting with Denys-Drash syndrome and cortical atrophy.
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A novel WT1 missense mutation presenting with Denys-Drash syndrome and cortical atrophy.
A novel WT1 missense mutation presenting with Denys-Drash syndrome and cortical atrophy. Nephrol Dial Transplant. 2006 Feb; 21(2):518-21.
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PubMed
subject areas
Atrophy
Child, Preschool
Corpus Callosum
Denys-Drash Syndrome
Follow-Up Studies
Humans
Infant
Karyotyping
Male
Mutation, Missense
WT1 Proteins
authors with profiles
Valerie Schumacher, Ph.D.