ArticleHuman genetics2019
A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss.
Claire J Sineni et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
16 papers cite it
this papercites it
ArticleHuman genetics2019
Claire J Sineni et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.