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Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families
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 DonatoVolume:
25
Language:
english
Pages:
8
DOI:
10.1007/s10072-004-0246-z
Date:
July, 2004
File:
PDF, 153 KB
english, 2004