A further observation of corneal dystrophy and perceptive deafness in two siblings.
about
Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome)Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophySlc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities.The genetics of Fuchs' corneal dystrophy
P2860
A further observation of corneal dystrophy and perceptive deafness in two siblings.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh-hant
name
A further observation of corneal dystrophy and perceptive deafness in two siblings.
@en
A further observation of corneal dystrophy and perceptive deafness in two siblings.
@nl
type
label
A further observation of corneal dystrophy and perceptive deafness in two siblings.
@en
A further observation of corneal dystrophy and perceptive deafness in two siblings.
@nl
prefLabel
A further observation of corneal dystrophy and perceptive deafness in two siblings.
@en
A further observation of corneal dystrophy and perceptive deafness in two siblings.
@nl
P2093
P2860
P1433
P1476
A further observation of corneal dystrophy and perceptive deafness in two siblings.
@en
P2093
P2860
P356
10.3109/13816819709057120
P577
1997-06-01T00:00:00Z