A Novel de novo Mutation in CEACAM16 Associated with Postlingual Hearing Impairment

Mutations in CEACAM16 cause autosomal dominant nonsyndromic hearing loss (DFNA4B). So far, 2 families have been reported with segregating missense mutations, both in the immunoglobulin constant domain A of the CEACAM16 protein. In this study, we used the TruSight One panel to investigate a parent-ch...

Full description

Saved in:
Bibliographic Details
Published in:Mol Syndromol
Main Authors: Hofrichter, Michaela A.H., Nanda, Indrajit, Gräf, Jens, Schröder, Jörg, Shehata-Dieler, Wafaa, Vona, Barbara, Haaf, Thomas
Format: Artigo
Language:Inglês
Published: S. Karger AG 2015
Subjects:
Original Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4662267/
https://ncbi.nlm.nih.gov/pubmed/26648831
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000439576
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items