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01-07-2004 | ORIGINAL

Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families

Authors: C. Mariotti, C. Gellera, M. Rimoldi, R. Mineri, G. Uziel, G. Zorzi, D. Pareyson, G. Piccolo, D. Gambi, S. Piacentini, F. Squitieri, R. Capra, B. Castellotti, S. Di Donato

Published in: Neurological Sciences | Issue 3/2004

Title: Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families
Authors: C. Mariotti
C. Gellera
M. Rimoldi
R. Mineri
G. Uziel
G. Zorzi
D. Pareyson
G. Piccolo
D. Gambi
S. Piacentini
F. Squitieri
R. Capra
B. Castellotti
S. Di Donato
Publication date: 01-07-2004
Publisher: Springer-Verlag
Published in: Neurological Sciences / Issue 3/2004
Print ISSN: 1590-1874
Electronic ISSN: 1590-3478
DOI: https://doi.org/10.1007/s10072-004-0246-z

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Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families

Keynote webinar | Spotlight on medication adherence

Springer Medicine

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