Identification of a Large DNAJB2 Deletion in a Family with Spinal Muscular Atrophy and Parkinsonism.
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Chaperonopathies: Spotlight on Hereditary Motor NeuropathiesProtein kinase CK2 modulates HSJ1 function through phosphorylation of the UIM2 domain.Autophagy as an Emerging Common Pathomechanism in Inherited Peripheral Neuropathies.The Role of Co-chaperones in Synaptic Proteostasis and Neurodegenerative Disease.Whole genome sequencing identifies a novel homozygous exon deletion in the NT5C2 gene in a family with intellectual disability and spastic paraplegia.A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations.DNAJ Proteins in neurodegeneration: essential and protective factors.
P2860
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P2860
Identification of a Large DNAJB2 Deletion in a Family with Spinal Muscular Atrophy and Parkinsonism.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Identification of a Large DNAJ ...... ular Atrophy and Parkinsonism.
@en
Identification of a Large DNAJ ...... ular Atrophy and Parkinsonism.
@nl
type
label
Identification of a Large DNAJ ...... ular Atrophy and Parkinsonism.
@en
Identification of a Large DNAJ ...... ular Atrophy and Parkinsonism.
@nl
prefLabel
Identification of a Large DNAJ ...... ular Atrophy and Parkinsonism.
@en
Identification of a Large DNAJ ...... ular Atrophy and Parkinsonism.
@nl
P2093
P2860
P356
P1433
P1476
Identification of a Large DNAJ ...... cular Atrophy and Parkinsonism
@en
P2093
Abbas Tafakhori
Coro Paisán-Ruiz
Hossein Darvish
Ruth H Walker
Saghar Ghasemi Firouzabadi
Shaghyegh Taghavi
P2860
P304
P356
10.1002/HUMU.23055
P577
2016-08-21T00:00:00Z