Login / Signup

A novel WT1 gene mutation in a chinese girl with denys-drash syndrome.

Fa-Liang WangJiabin CaiJinhu WangMin HeJunqing MaoKun ZhuManli ZhaoZhonghai GuanLinjie LiHongchuan JinQiang Shu
Published in: Journal of clinical laboratory analysis (2021)
The uncommon missense mutation (c.1420C>T, p.His474 Tyr) in the WT1 gene may be a crucial marker in DDS.
Keyphrases
  • intellectual disability
  • copy number
  • genome wide
  • case report
  • genome wide identification
  • gene expression