Hereditary protein C deficiency associated with riboflavin-responsive lipid storage myopathy

European Journal of Neurology

Volumn 3, Issue 1, 1996, Pages 61-65

  Vergani, L ^a   Angelini, C ^a   Pegoraro, E ^a   Cadaldini, M ^a   Simioni, P ^b   Girolami, A ^b   Turnbull, D M ^b  

^a UNIVERSITY OF PADOVA   (Italy)

^b Department of Internal Medicine ^*  (United Kingdom)

Author keywords

acylCoA dehydrogenase; carnitine; lipid myopathy; protein C deficiency

Indexed keywords

ACYL COENZYME A DEHYDROGENASE; CARNITINE; PROTEIN C; RIBOFLAVIN; WARFARIN;

ADOLESCENT; ARTICLE; CASE REPORT; HEREDITY; HUMAN; HUMAN TISSUE; LIPIDOSIS; MALE; PRIORITY JOURNAL; PROTEIN C DEFICIENCY;

EID: 0029915789     PISSN: 13515101     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1468-1331.1996.tb00191.x     Document Type: Article

References (8)

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