A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation (Q24337631)
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Current Data About A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation
(P31) (Q13442814)

(P50) (Q53816684)
(P1932) C Dionisi-Vici
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(P1932) E Bertini
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(Q73596856)
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(P304) 1966-8

(P407) (Q1860)

(P433) 12

(P478) 59

(P577) Tuesday, December 24, 2002

(P921) (Q822050)

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(P248)

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(P248)

(Q21110147)
(P248)

(Q21108564)
(P248)

(Q14860504)
(P248)

(P1433) (Q1161692)

(P1476) "A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation" (language: en)

(P2093) A Fogli
(P1545) 1

F Deodato
(P1545) 3

A Bartuli
(P1545) 4

O Boespflug-Tanguy
(P1545) 5

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