Functional analysis of recently identified mutations in eukaryotic translation initiation factor 2Bε (eIF2Bε) identified in Chinese patients with vanishing white matter disease
スポンサーリンク
概要
著者
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Leng Xuerong
Pediatric Department Peking University First Hospital
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Wang Xuemin
Human Genetics Division University Of Southampton Duthie Building Southampton General Hospital
関連論文
- Functional analysis of recently identified mutations in eukaryotic translation initiation factor 2Bε (eIF2Bε) identified in Chinese patients with vanishing white matter disease
- Functional analysis of recently identified mutations in eukaryotic translation initiation factor 2Bε (eIF2Bε) identified in Chinese patients with vanishing white matter disease
- Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease