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Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype.

Jiaxin HeQiang LiuWeili WangLilan SuLanlan MengChen TanHuan ZhangQianjun ZhangGuangxiu LuJuan DuGe LinChaofeng TuYue-Qiu Tan
Published in: Clinical genetics (2022)
A: Characteristics of spermatozoa in asthenoteratozoospermia affected man. B: Pedigree and Sanger sequencing analysis of the family. C: The effect of the missense variant in the CCIN gene. This article is protected by copyright. All rights reserved.
Keyphrases
  • intellectual disability
  • copy number
  • single cell
  • genome wide
  • polycystic ovary syndrome
  • type diabetes
  • genome wide identification
  • gene expression
  • metabolic syndrome
  • adipose tissue
  • skeletal muscle