病例报告:新型CNGA3复合异合体变体在一个家庭的三名患者中引起色素

Xiaoqiang Zhou1, Yasi Zhou2, Shuijuan Wu1

  • 1Prenatal Diagnosis Center, Foshan Women and Children Hospital, Foshan, Guangdong, China.

Frontiers in genetics
|December 16, 2024
PubMed
概括

研究人员在CNGA3基因中发现了一种新的遗传变异,该变异在一个中国家庭中导致了色素. 这一发现促进了对遗传性视网膜疾病的理解,以及对阿克罗马托普西亚的遗传诊断.

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