Multiple Sclerosis and EIF2B5: A Paradox or a Missing Link.

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Multiple Sclerosis and EIF2B5: A Paradox or a Missing Link.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Multiple Sclerosis and EIF2B5: A Paradox or a Missing Link.

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Multiple Sclerosis and EIF2B5: A Paradox or a Missing Link.

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Multiple Sclerosis and EIF2B5: A Paradox or a Missing Link.

@en

Multiple Sclerosis and EIF2B5: A Paradox or a Missing Link.

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Multiple Sclerosis and EIF2B5: A Paradox or a Missing Link.

@en

Multiple Sclerosis and EIF2B5: A Paradox or a Missing Link.

@nl

P1476

Multiple Sclerosis and EIF2B5: A Paradox or a Missing Link.

@en

P2093

Ehtishamul Haq

http://www.w3.org/2001/XMLSchema#string

Insha Zahoor

http://www.w3.org/2001/XMLSchema#string

Ravouf Asimi

http://www.w3.org/2001/XMLSchema#string

P2860

Vitamin D: An Evidence-Based Review

Defining the clinical course of multiple sclerosis: Results of an international survey

The prevalence of multiple sclerosis in the world: an update

Environmental risk factors for multiple sclerosis. Part I: The role of infection

Eukaryotic initiation factor 2B: identification of multiple phosphorylation sites in the epsilon-subunit and their functions in vivo

Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans.

Identification of domains and residues within the epsilon subunit of eukaryotic translation initiation factor 2B (eIF2Bepsilon) required for guanine nucleotide exchange reveals a novel activation function promoted by eIF2B complex formation

Diagnostic criteria for multiple sclerosis: 2010 revisions to the McDonald criteria

Epidemiology and genetic aspects of multiple sclerosis in India

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

P304

57-64

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P31

scholarly article

P356

10.1007/978-3-319-47861-6_5

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P407

English

P478

958

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P577

2017-01-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

28093708

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P921

multiple sclerosis