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Novel biallelic mutations in TTC29 cause asthenoteratospermia and male infertility.

Siyu DaiYan LiangMohan LiuYanting YangHongqian LiuYing Shen
Published in: Molecular genetics & genomic medicine (2022)
Our study revealed the novel biallelic mutations in TTC29 in a MMAF patient, which findings expand the mutational spectrum of TTC29 and further contribute to the diagnosis, genetic counseling, and prognosis of male infertility.
Keyphrases
  • intellectual disability
  • case report
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