Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
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A Chinese family with Axenfeld-Rieger syndrome: report of the clinical and genetic findingsThe rare Axenfeld-Rieger syndrome with systemic anomalies: A case report and brief review of literatureA Novel Mutation in PITX2 in a Patient with Axenfeld-Rieger Syndrome.Molecular Genetics of Pigment Dispersion Syndrome and Pigmentary Glaucoma: New Insights into Mechanisms.Accurate prediction of functional, structural, and stability changes in PITX2 mutations using in silico bioinformatics algorithms.
P2860
Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh-hant
name
Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
@en
Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
@nl
type
label
Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
@en
Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
@nl
prefLabel
Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
@en
Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
@nl
P2093
P2860
P356
P1433
P1476
Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndrome
@en
P2093
Ebtesam M Abdalla
Michael A Walter
Morteza Seifi
Sherry A M Taylor
P2860
P304
P356
10.1111/AOS.13030
P577
2016-03-24T00:00:00Z