Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter.

LEEGWATER P A J; VERMEULEN G; KOENST A A M; NAIDU S; MULDERS J; VISSER A; MOBACH D; FRANTS R R; VAN DER KNAAP M S

Art

J-GLOBAL ID：200902190844271897 Reference number：02A0120995

Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter.

翻訳開始因子eIF2Bのサブユニットは白質の喪失を伴う白質脳症の変異体である

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Material：
Volume： 29 Issue： 4 Page： 383-388 Publication year： Dec. 10, 2001
JST Material Number： W0430A ISSN： 1061-4036 Document type： Article
Article type：原著論文 Country of issue： United States (USA) Language： ENGLISH (EN)

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Congenital diseases,deformities in general. , Nervous system diseases , Genetic variation , Biological function , Gene expression

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