1.
Rev. neurol. (Ed. impr.)
; 55(4): 250-251, 16 ago., 2012. ilus
Article
in Spanish
| IBECS
| ID: ibc-101837
ABSTRACT
No disponible
Subject(s)
Humans , Male , Child , Cockayne Syndrome/genetics , Chromosome Disorders/complications , Mutation/genetics , Hearing Loss/etiology , Retinitis Pigmentosa/etiology
2.
Rev Neurol
; 55(4): 250-1, 2012 Aug 16.
Article
in Spanish
| MEDLINE
| ID: mdl-22829088