Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families.
Mariotti, C
Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families. [electronic resource] - Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology Jul 2004 - 130-7 p. digital
Publication Type: Journal Article
1590-1874
10.1007/s10072-004-0246-z doi
Adolescent
Adult
Ataxia--diagnosis
Carrier Proteins--genetics
Female
Follow-Up Studies
Humans
Italy
Male
Middle Aged
Mutation
Nervous System Diseases--diagnosis
Pedigree
Phenotype
Vitamin E--therapeutic use
Vitamin E Deficiency--diagnosis
Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families. [electronic resource] - Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology Jul 2004 - 130-7 p. digital
Publication Type: Journal Article
1590-1874
10.1007/s10072-004-0246-z doi
Adolescent
Adult
Ataxia--diagnosis
Carrier Proteins--genetics
Female
Follow-Up Studies
Humans
Italy
Male
Middle Aged
Mutation
Nervous System Diseases--diagnosis
Pedigree
Phenotype
Vitamin E--therapeutic use
Vitamin E Deficiency--diagnosis