类似于努南综合征的表型与ERF框架转移变异相关
Yasuhiro Hirano1,2, Yukiko Kuroda3, Yumi Enomoto4
1Department of Pediatrics, Hiratsuka City Hospital, Hiratsuka, Kanagawa, Japan.
American journal of medical genetics. Part A
|May 14, 2024
概括
努南综合症,一个RASopathy,呈现出不同的特征. 一个新的ERF基因变异在一个患有诺南综合征样症状的家庭中被发现,这表明ERF变异有助于这种疾病.
科学领域:
- 遗传学 遗传学 是一个
- 分子生物学分子生物学
- 发展生物学 发展生物学
背景情况:
- 努南综合征是一种RAS病,在80-90%的病例中已知遗传原因.
- ETS2抑制因子 (ERF) 变体与综合征性关节缩症有关.
- 诺南综合征背后的分子机制仍然不完全理解.
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