Pelletier, J., et al. “A Novel Mutation H373Y in the Wilms’ Tumor Suppressor Gene, WT1, Associated With Denys-Drash Syndrome”. Human Heredity, vol. 46, no. 6, 1996, pp. 336-8, https://doi.org/10.1159/000154374.

Genre

  • Journal Article
Contributors
Author: Pelletier, J.
Author: Tieder, M.
Author: Bistritzer, T.
Author: Aladjem, M. M.
Author: Ghahremani, M.
Author: Chan, Catherine B.
Date Issued
1996
Note

Department of Biochemistry, McGill University, Montreal, Canada.

SWITZERLAND

LR: 20061115; PUBM: Print; JID: 0200525; 55520-40-6 (Tyrosine); 71-00-1 (Histidine); ppublish

Source type: Electronic(1)

Language

  • English

Subjects

  • Point Mutation
  • Humans
  • Pseudohermaphroditism/genetics
  • Genes, Wilms Tumor
  • Nephrotic Syndrome/genetics
  • Male
  • Tyrosine/genetics
  • Polymorphism, Single-Stranded Conformational
  • Histidine/genetics
  • polymerase chain reaction
  • Child, Preschool
Page range
336-338
Host Title
Human Heredity
Host Abbreviated Title
Hum.Hered.
Volume
46
Issue
6
ISSN
0001-5652
DOI
https://doi.org/10.1159/000154374

Department