与凯珀特综合征和眼点性生殖相关的GPC4截断变异
Yukiko Kuroda1, Takeshi Uehara1, Yumi Enomoto2
1Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.
American journal of medical genetics. Part A
|June 26, 2024
概括
眼点性生殖,一种罕见的疾病,可能与导致凯珀特综合征的glypican 4 (GPC4) 基因变异有关. 这一发现扩大了对GPC4的理解.
科学领域:
- 遗传学和发育生物学
- 眼科和脸部发育
背景情况:
- 眼点性生殖是一种非常罕见的先天性疾病,遗传病因不明.
- 凯珀特综合征是一种罕见的遗传性疾病,其特点是特定的面异常,发育迟缓和智力障碍.
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