KRT12 mutations and in vivo confocal microscopy in two Japanese families with Meesmann corneal dystrophy.
about
Characteristics of corneal dystrophies: a review from clinical, histological and genetic perspectivesIdentification of presumed pathogenic KRT3 and KRT12 gene mutations associated with Meesmann corneal dystrophy.Comprehensive analysis of genetic variations in strictly-defined Leber congenital amaurosis with whole-exome sequencing in Chinese.Mutation analysis of TGFBI and KRT12 in a case of concomitant keratoconus and granular corneal dystrophy.
P2860
KRT12 mutations and in vivo confocal microscopy in two Japanese families with Meesmann corneal dystrophy.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
KRT12 mutations and in vivo co ...... th Meesmann corneal dystrophy.
@en
KRT12 mutations and in vivo co ...... th Meesmann corneal dystrophy.
@nl
type
label
KRT12 mutations and in vivo co ...... th Meesmann corneal dystrophy.
@en
KRT12 mutations and in vivo co ...... th Meesmann corneal dystrophy.
@nl
prefLabel
KRT12 mutations and in vivo co ...... th Meesmann corneal dystrophy.
@en
KRT12 mutations and in vivo co ...... th Meesmann corneal dystrophy.
@nl
P2093
P1476
KRT12 mutations and in vivo co ...... th Meesmann corneal dystrophy.
@en
P2093
Hiroshi Tsuneoka
Hisashi Yamada
Jun Shimazaki
Kazuo Tsubota
Kenji Ohno
Mikihide Ogasawara
Murat Dogru
Takaaki Hayashi
Tetsuya Kawakita
Yukihiro Matsumoto
P304
P356
10.1016/J.AJO.2013.08.008
P407
P577
2013-10-05T00:00:00Z