Mariotti, C <br/><br/>
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 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1590-1874 
<br/><br/><label>Standard No.: </label>10.1007/s10072-004-0246-z  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Ataxia--diagnosis<br/>Carrier Proteins--genetics<br/>Female<br/>Follow-Up Studies<br/>Humans<br/>Italy<br/>Male<br/>Middle Aged<br/>Mutation<br/>Nervous System Diseases--diagnosis<br/>Pedigree<br/>Phenotype<br/>Vitamin E--therapeutic use<br/>Vitamin E Deficiency--diagnosis