Novel PITX2c loss-of-function mutations associated with complex congenital heart disease.
about
PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger SyndromeTBX1 loss-of-function mutation contributes to congenital conotruncal defects.Multiple Roles of Pitx2 in Cardiac Development and Disease.Accurate prediction of functional, structural, and stability changes in PITX2 mutations using in silico bioinformatics algorithms.
P2860
Novel PITX2c loss-of-function mutations associated with complex congenital heart disease.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
Novel PITX2c loss-of-function mutations associated with complex congenital heart disease.
@en
Novel PITX2c loss-of-function mutations associated with complex congenital heart disease.
@nl
type
label
Novel PITX2c loss-of-function mutations associated with complex congenital heart disease.
@en
Novel PITX2c loss-of-function mutations associated with complex congenital heart disease.
@nl
prefLabel
Novel PITX2c loss-of-function mutations associated with complex congenital heart disease.
@en
Novel PITX2c loss-of-function mutations associated with complex congenital heart disease.
@nl
P2093
P356
P1476
Novel PITX2c loss-of-function mutations associated with complex congenital heart disease.
@en
P2093
Xiao-Hui Gong
Yi-Qing Yang
P304
P356
10.3892/IJMM.2014.1689
P577
2014-03-07T00:00:00Z