Whole-exome sequencing identifies a de novo TUBA1A mutation in a patient with sporadic malformations of cortical development: a case report.
about
TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis.MNRR1, a Biorganellar Regulator of Mitochondria.The function of sperm-associated antigen 6 in neuronal proliferation and differentiation.The α-Tubulin gene TUBA1A in Brain Development: A Key Ingredient in the Neuronal Isotype Blend.A novel TUBB3 mutation in a sporadic patient with asymmetric cortical dysplasia.
P2860
Whole-exome sequencing identifies a de novo TUBA1A mutation in a patient with sporadic malformations of cortical development: a case report.
description
2014 nî lūn-bûn
@nan
2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
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
name
Whole-exome sequencing identif ...... al development: a case report.
@ast
Whole-exome sequencing identif ...... al development: a case report.
@en
type
label
Whole-exome sequencing identif ...... al development: a case report.
@ast
Whole-exome sequencing identif ...... al development: a case report.
@en
prefLabel
Whole-exome sequencing identif ...... al development: a case report.
@ast
Whole-exome sequencing identif ...... al development: a case report.
@en
P2093
P2860
P356
P1433
P1476
Whole-exome sequencing identif ...... al development: a case report.
@en
P2093
Akira Saito
Aya Narita
Keiko Shimojima
Toshiyuki Yamamoto
Yoshihiro Maegaki
P2860
P2888
P356
10.1186/1756-0500-7-465
P577
2014-07-22T00:00:00Z
P5875
P6179
1032956904