ArticleHuman genetics2018
ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss.
Wu Li et al.PubMed ↗Publisher ↗
No numbers read from the abstract.
16 papers cite it
this papercites it
ArticleHuman genetics2018
Wu Li et al.PubMed ↗Publisher ↗
No numbers read from the abstract.