A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation
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The emerging role of guanine nucleotide exchange factors in ALS and other neurodegenerative diseases.Adult-onset vanishing white matter disease as differential diagnosis of primary progressive multiple sclerosis: a case report.Automated segmentation reveals silent radiographic progression in adult-onset vanishing white-matter disease.Identification of variants in pleiotropic genes causing "isolated" premature ovarian insufficiency: implications for medical practice
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A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation
description
im Oktober 2012 veröffentlichter wissenschaftlicher Artikel
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scientific article published on 31 October 2012
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wetenschappelijk artikel
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наукова стаття, опублікована в жовтні 2012
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name
A 66-year-old patient with van ...... the p.Ala87Val EIF2B3 mutation
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A 66-year-old patient with van ...... the p.Ala87Val EIF2B3 mutation
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type
label
A 66-year-old patient with van ...... the p.Ala87Val EIF2B3 mutation
@en
A 66-year-old patient with van ...... the p.Ala87Val EIF2B3 mutation
@nl
prefLabel
A 66-year-old patient with van ...... the p.Ala87Val EIF2B3 mutation
@en
A 66-year-old patient with van ...... the p.Ala87Val EIF2B3 mutation
@nl
P2093
P50
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A 66-year-old patient with van ...... the p.Ala87Val EIF2B3 mutation
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P2093
Erika Tenderini
Francesca Jacini
Mario Rango
Milena De Riz
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P356
10.1212/WNL.0B013E3182749EDC
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P50
P577
2012-10-31T00:00:00Z