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Case report: Biallelic variants in POLR3B gene lead to 4H leukodystrophy from the study of brother and sister.

Hengzhou BaiDingming LiYi ZhengXiaoHui Jiang
Published in: Medicine (2022)
The exploration of molecular functions and genetic counseling are crucial for further diagnosis and treatment of POLR3-related leukodystrophy.
Keyphrases
  • copy number
  • case report
  • genome wide
  • intellectual disability
  • gene expression
  • autism spectrum disorder
  • hepatitis c virus
  • genome wide identification
  • drug induced