Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease. [electronic resource]
Producer: 20100203Description: 74-7 p. digitalISSN:- 1435-232X
- Amino Acid Sequence
- Asian People -- genetics
- Child
- Child, Preschool
- Conserved Sequence
- DNA Mutational Analysis
- Eukaryotic Initiation Factor-2B -- chemistry
- Female
- Humans
- Infant
- Leukoencephalopathies -- genetics
- Magnetic Resonance Imaging
- Male
- Molecular Sequence Data
- Mutation -- genetics
- Mutation, Missense -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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