EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss
δημοσιεύθηκε στο: Orphanet Journal of Rare Diseases
date of publication: 2015-08-19
main subject: απώλεια ακοής
Cites articles 35
- 2013-01-25
- 2001-01-01
Date
Title
Article - wd:Q35964651