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