Massively parallel DNA sequencing successfully identified seven families with deafness-associated MYO6 mutations: the mutational spectrum and clinical characteristics.
about
A Comprehensive Study on the Etiology of Patients Receiving Cochlear Implantation With Special Emphasis on Genetic Epidemiology.Navigating genetic diagnostics in patients with hearing loss.Exome Sequencing Identifies a Novel Nonsense Mutation of MYO6 as the Cause of Deafness in a Brazilian Family.Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction.
P2860
Massively parallel DNA sequencing successfully identified seven families with deafness-associated MYO6 mutations: the mutational spectrum and clinical characteristics.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh-hant
name
Massively parallel DNA sequenc ...... and clinical characteristics.
@en
Massively parallel DNA sequenc ...... and clinical characteristics.
@nl
type
label
Massively parallel DNA sequenc ...... and clinical characteristics.
@en
Massively parallel DNA sequenc ...... and clinical characteristics.
@nl
prefLabel
Massively parallel DNA sequenc ...... and clinical characteristics.
@en
Massively parallel DNA sequenc ...... and clinical characteristics.
@nl
P2093
P2860
P356
P1476
Massively parallel DNA sequenc ...... and clinical characteristics.
@en
P2093
Kozo Kumakawa
Maiko Miyagawa
Shin-Ichi Usami
P2860
P304
P356
10.1177/0003489415575055
P478
124 Suppl 1
P577
2015-05-01T00:00:00Z