PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome
about
The Dorsal Mesenchymal Protrusion and the Pathogenesis of Atrioventricular Septal Defects.Translational issues for human corneal endothelial tissue engineering.An update on the molecular diagnosis of congenital heart disease: focus on loss-of-function mutations.A Novel Mutation in PITX2 in a Patient with Axenfeld-Rieger Syndrome.Current Perspectives in Cardiac Laterality.Multiple Roles of Pitx2 in Cardiac Development and Disease.Myocardial transcription factors in diastolic dysfunction: clues for model systems and disease.HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot.
P2860
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P2860
PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome
description
2015 nî lūn-bûn
@nan
2015 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի ապրիլին 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
PITX2 Loss-of-Function Mutatio ...... t and Axenfeld-Rieger Syndrome
@ast
PITX2 Loss-of-Function Mutatio ...... t and Axenfeld-Rieger Syndrome
@en
type
label
PITX2 Loss-of-Function Mutatio ...... t and Axenfeld-Rieger Syndrome
@ast
PITX2 Loss-of-Function Mutatio ...... t and Axenfeld-Rieger Syndrome
@en
prefLabel
PITX2 Loss-of-Function Mutatio ...... t and Axenfeld-Rieger Syndrome
@ast
PITX2 Loss-of-Function Mutatio ...... t and Axenfeld-Rieger Syndrome
@en
P2093
P2860
P1433
P1476
PITX2 Loss-of-Function Mutatio ...... t and Axenfeld-Rieger Syndrome
@en
P2093
Cui-Mei Zhao
Lu-Ying Peng
Xian-Ling Zhang
Xing-Biao Qiu
Xing-Yuan Liu
Yi-Qing Yang
P2860
P304
P356
10.1371/JOURNAL.PONE.0124409
P407
P577
2015-04-20T00:00:00Z