A novel PITX2 mutation in a Chinese family with Axenfeld-Rieger syndrome.
about
The Pitx2c N-terminal domain is a critical interaction domain required for asymmetric morphogenesis.Identification of a novel frameshift mutation in PITX2 gene in a Chinese family with Axenfeld-Rieger syndrome.Structural and biophysical insights into the ligand-free Pitx2 homeodomain and a ring dermoid of the cornea inducing homeodomain mutant.Magnetic resonance imaging findings in Axenfeld-Rieger syndrome.Accurate prediction of functional, structural, and stability changes in PITX2 mutations using in silico bioinformatics algorithms.
P2860
A novel PITX2 mutation in a Chinese family with Axenfeld-Rieger syndrome.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
A novel PITX2 mutation in a Chinese family with Axenfeld-Rieger syndrome.
@en
type
label
A novel PITX2 mutation in a Chinese family with Axenfeld-Rieger syndrome.
@en
prefLabel
A novel PITX2 mutation in a Chinese family with Axenfeld-Rieger syndrome.
@en
P2093
P2860
P1433
P1476
A novel PITX2 mutation in a Chinese family with Axenfeld-Rieger syndrome
@en
P2093
P2860
P304
P577
2008-12-05T00:00:00Z