TSEN54,

Bayoumi A Emam1, Mohamed S Abdel-Hamid2, Maha Eid3

  • 1Department of Clinical Genetics, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.

Molecular syndromology
|December 5, 2024
PubMed
概括

基因查发现了TSEN54基因变异c.919G>T (p.A307S) 在20%的埃及脑小骨缺血症 (PCH) 患者中. 这一发现有助于诊断罕见的PCH疾病和遗传咨询.