Functional analysis of FOXE3 mutations causing dominant and recessive ocular anterior segment disease
about
FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1Novel FOXC2 Mutation in Hereditary Distichiasis Impairs DNA-Binding Activity and Transcriptional Activation.Mutation update of transcription factor genes FOXE3, HSF4, MAF, and PITX3 causing cataracts and other developmental ocular defects.
P2860
Functional analysis of FOXE3 mutations causing dominant and recessive ocular anterior segment disease
description
2015 nî lūn-bûn
@nan
2015 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի մարտին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Functional analysis of FOXE3 m ...... cular anterior segment disease
@ast
Functional analysis of FOXE3 m ...... cular anterior segment disease
@en
Functional analysis of FOXE3 m ...... cular anterior segment disease
@en-gb
Functional analysis of FOXE3 m ...... cular anterior segment disease
@nl
type
label
Functional analysis of FOXE3 m ...... cular anterior segment disease
@ast
Functional analysis of FOXE3 m ...... cular anterior segment disease
@en
Functional analysis of FOXE3 m ...... cular anterior segment disease
@en-gb
Functional analysis of FOXE3 m ...... cular anterior segment disease
@nl
prefLabel
Functional analysis of FOXE3 m ...... cular anterior segment disease
@ast
Functional analysis of FOXE3 m ...... cular anterior segment disease
@en
Functional analysis of FOXE3 m ...... cular anterior segment disease
@en-gb
Functional analysis of FOXE3 m ...... cular anterior segment disease
@nl
P2093
P2860
P3181
P356
P1433
P1476
Functional analysis of FOXE3 m ...... cular anterior segment disease
@en
P2093
Daniel Kelberman
Ken K Nischal
Laura Williamson
Lily Islam
Maria Bitner Glindzicz
Nicola Lewis
P2860
P304
P3181
P356
10.1002/HUMU.22741
P407
P577
2015-03-01T00:00:00Z