DNAH11 c.3853-24C>T

Variant ID: 7-21654708-C-T

NM_001277115.1(DNAH11):c.3853-24C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Case Report: The novel hemizygous mutation in the SSR4 gene caused congenital disorder of glycosylation type iy: A case study and literature review.

Frontiers In Genetics
Wang, Jun J; Gou, Xingqing X; Wang, Xiyi X; Zhang, Jing J; Zhao, Nan N; Wang, Xiaohong X
Publication Date: 2022

Variant appearance in text: DNAH11: 3853-24C>T; rs182638542
PubMed Link: 36386804
Variant Present in the following documents:
  • Table1.xls, sheet 1
View BVdb publication page