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

✍ Scribed by 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

• Publisher: Springer Milan
• Year: 2004
• Tongue: English
• Weight: 153 KB
• Volume: 25
• Category: Article
• ISSN: 1590-1874
• DOI: 10.1007/s10072-004-0246-z