Adult-onset autosomal dominant spastic paraplegia linked to a GTPase-effector domain mutation of dynamin 2.
about
Hereditary Spastic Paraplegia: Clinical and Genetic Hallmarks.Allele-specific silencing therapy for Dynamin 2-related dominant centronuclear myopathy.Phenotype variability and histopathological findings in patients with a novel DNM2 mutation.Loss of Dynamin 2 GTPase function results in microcytic anaemia.Differential Expression of Several miRNAs and the Host Genes AATK and DNM2 in Leukocytes of Sporadic ALS Patients.
P2860
Adult-onset autosomal dominant spastic paraplegia linked to a GTPase-effector domain mutation of dynamin 2.
description
2015 nî lūn-bûn
@nan
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
2015年论文
@zh
2015年论文
@zh-cn
name
Adult-onset autosomal dominant ...... domain mutation of dynamin 2.
@ast
Adult-onset autosomal dominant ...... domain mutation of dynamin 2.
@en
type
label
Adult-onset autosomal dominant ...... domain mutation of dynamin 2.
@ast
Adult-onset autosomal dominant ...... domain mutation of dynamin 2.
@en
prefLabel
Adult-onset autosomal dominant ...... domain mutation of dynamin 2.
@ast
Adult-onset autosomal dominant ...... domain mutation of dynamin 2.
@en
P2093
P2860
P1433
P1476
Adult-onset autosomal dominant ...... domain mutation of dynamin 2.
@en
P2093
Al'bina P Danilova
Anastasia N Ylakhova
Camilo Toro
Fyodor A Platonov
Jenny E Hinshaw
Lev G Goldfarb
Margarita P Diachkovskaya
Neil M Renwick
Nyamkhishig Sambuughin
Raisa S Nikitina
P2860
P2888
P356
10.1186/S12883-015-0481-3
P577
2015-10-30T00:00:00Z
P5875
P6179
1016400122