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

Author： 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.  

Publisher： Springer Publishing Company

ISSN： 1590-1874

Source： Neurological Sciences, Vol.25, Iss.3, 2004-07, pp. : 130-137

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