Human Genome Epidemiology Literature Finder
Records 1 - 1 (of 1 Records) |
Query Trace: Hearing and CABP2[original query] |
---|
A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family. Audiology & neuro-otology 2019 10 24 (5): 258-263. Koohiyan Mahbobeh, Noori-Daloii Mohammad Reza, Hashemzadeh-Chaleshtori Morteza, Salehi Mansoor, Abtahi Hamidreza, Tabatabaiefar Mohammad Am |
- Page last reviewed:Feb 1, 2024
- Page last updated:Mar 25, 2024
- Content source: