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Mutation of c.244G>T in NR5A1 gene causing 46, XY DSD by affecting RNA splicing.

Bingqing YuYinjie GaoJiangfeng MaoXi WangMin NieXueyan Wu
Published in: Orphanet journal of rare diseases (2021)
Mutation of c.244G>T in NR5A1 results in 46, XY DSD by inducing abnormal splicing of NR5A1 RNA instead of amino acid substitution of NR5A1.
Keyphrases
  • amino acid
  • genome wide
  • copy number
  • gene expression
  • dna methylation
  • transcription factor
  • genome wide identification