A novel splice site mutation in the EYA1 gene in a Korean family with branchio-oto (BO) syndrome.
about
Mutational analysis of EYA1, SIX1 and SIX5 genes and strategies for management of hearing loss in patients with BOR/BO syndrome.Identification of a novel nonsynonymous mutation of EYA1 disrupting splice site in a Korean patient with BOR syndrome.A de novo and novel mutation in the EYA1 gene in a Chinese child with branchio-oto-renal syndrome.The first case of NSHL by direct impression on EYA1 gene and identification of one novel mutation in MYO7A in the Iranian families.Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndrome.
P2860
A novel splice site mutation in the EYA1 gene in a Korean family with branchio-oto (BO) syndrome.
description
2009 nî lūn-bûn
@nan
2009年の論文
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2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
A novel splice site mutation i ...... th branchio-oto (BO) syndrome.
@en
A novel splice site mutation in the EYA1 gene in a Korean family with branchio-oto
@nl
type
label
A novel splice site mutation i ...... th branchio-oto (BO) syndrome.
@en
A novel splice site mutation in the EYA1 gene in a Korean family with branchio-oto
@nl
prefLabel
A novel splice site mutation i ...... th branchio-oto (BO) syndrome.
@en
A novel splice site mutation in the EYA1 gene in a Korean family with branchio-oto
@nl
P2093
P2860
P1476
A novel splice site mutation i ...... th branchio-oto (BO) syndrome.
@en
P2093
Hee-Jin Kim
Min-Jung Kwon
Sung Hwa Hong
Sung Hyun Boo
Won-Ho Chung
Yang-Sun Cho
P2860
P304
P356
10.1080/00016480802342432
P407
P577
2009-06-01T00:00:00Z