A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation (Q24337631)

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A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation
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    A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation (English)
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    A Fogli
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    F Deodato
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    A Bartuli
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    O Boespflug-Tanguy
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    24 December 2002
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    59
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    12
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    1966-8
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