Journal article

Novel WT1 exon 9 mutation (D396Y) in a patient with early onset Denys Drash syndrome

Melissa Little, Gregory Carman, Eric Donaldson

Human Mutation | WILEY-BLACKWELL | Published : 2000

DOI: 10.1002/(SICI)1098-1004(200004)15:4<389::AID-HUMU29>3.0.CO;2-E

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Keywords

Tyrosine
Genetics & Heredity
Fatal Outcome
Dna-Binding Proteins
Syndrome
Amino Acid Substitution
Science & Technology
Child, Preschool
Wt1 Proteins
Male
Life Sciences & Biomedicine
Wt1
Denys Drash Syndrome
Humans
Transcription Factors
Mutation, Missense
Wilms' Tumour
Urogenital Abnormalities
Genes, Wilms Tumor
Exons
Infant, Newborn
Mesangial Sclerosis
Aspartic Acid