Familial ataxia with isolated vitamin E deficiency not due to mutation of α-TTP [8]

Journal of Neurology

Volumn 246, Issue 10, 1999, Pages 982-

  Shiojiri, T ^a   Yokota, T ^a   Fujimori, N ^a   Mizusawa, H ^a  

^a TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA TOCOPHEROL;

ADULT; ALPHA TOCOPHEROL DEFICIENCY; CASE REPORT; GENE; HEREDITARY ATAXIA; HUMAN; LETTER; MALE; PRIORITY JOURNAL;

ADULT; ATAXIA; CARRIER PROTEINS; HUMANS; MALE; MUTATION; VITAMIN E DEFICIENCY;

EID: 0032759266     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004150050499     Document Type: Letter

References (7)