Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course.
about
Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course.
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年學術文章
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2012年學術文章
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name
Vanishing white matter disease ...... early onset and a long course.
@en
Vanishing white matter disease ...... early onset and a long course.
@nl
type
label
Vanishing white matter disease ...... early onset and a long course.
@en
Vanishing white matter disease ...... early onset and a long course.
@nl
prefLabel
Vanishing white matter disease ...... early onset and a long course.
@en
Vanishing white matter disease ...... early onset and a long course.
@nl
P2093
P2860
P1476
Vanishing white matter disease ...... early onset and a long course
@en
P2093
Antonella Bacci
Luisa Sambati
Raffaele Agati
P2860
P2888
P304
P356
10.1007/S10072-012-1129-3
P577
2012-06-23T00:00:00Z