Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families
Titel:
Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families
Auteur:
Mariotti, C. Gellera, C. Rimoldi, M. Mineri, R. Uziel, G. Zorzi, G. Pareyson, D. Piccolo, G. Gambi, D. Piacentini, S. Squitieri, F. Capra, R. Castellotti, B. Donato, S. Di