DNAH11 c.704A>G ;(p.N235S)

Variant ID: 7-21599232-A-G

NM_001277115.1(DNAH11):c.704A>G;(p.N235S)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes.

Communications Biology
Wonkam, Ambroise A; Adadey, Samuel Mawuli SM; Schrauwen, Isabelle I; Aboagye, Elvis Twumasi ET; Wonkam-Tingang, Edmond E; Esoh, Kevin K; Popel, Kalinka K; Manyisa, Noluthando N; Jonas, Mario M; deKock, Carmen C; Nembaware, Victoria V; Cornejo Sanchez, Diana M DM; Bharadwaj, Thashi T; Nasir, Abdul A; Everard, Jenna L JL; Kadlubowska, Magda K MK; Nouel-Saied, Liz M LM; Acharya, Anushree A; Quaye, Osbourne O; Amedofu, Geoffrey K GK; Awandare, Gordon A GA; Leal, Suzanne M SM
Publication Date: 2022-04-19

Variant appearance in text: DNAH11: 704A>G
PubMed Link: 35440622
Variant Present in the following documents:
  • 42003_2022_Article_3326.pdf
View BVdb publication page