Detalhe da pesquisa
1.
Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cells.
Eur J Hum Genet
; 24(4): 542-9, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26173970
2.
Progressive hearing loss and vestibular dysfunction caused by a homozygous nonsense mutation in CLIC5.
Eur J Hum Genet
; 23(2): 189-94, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24781754
3.
Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families.
PLoS One
; 9(6): e100146, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24949729