在TXNDC15中出现新的同卵性突变,导致梅克尔综合征
1Reproductive Medical Center, Shenzhen Maternity & Child Healthcare Hospital, Shenzhen, People's Republic of China.
Molecular genetics & genomic medicine
|December 29, 2023
概括
梅克尔综合征 (MKS) 是一种严重的纤毛病. 在一个中国家庭中发现了TXNDC15基因的新同卵性突变,导致MKS14并有助于遗传咨询.
科学领域:
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
- 发展生物学 发展生物学
背景情况:
- 梅克尔综合征 (MKS) 是一种严重的自体递归纤毛病.
- 临床特征包括头脑,多囊性脏和多爪.
- TXNDC15基因突变与MKS相关.
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