Mitochondrial trifunctional protein deficiency: a rare cause of adult-onset rhabdomyolysis.

Muscle & nerve

Volumn 48, Issue 6, 2013, Pages 989-991

  Liewluck, Teerin ^a   Mundi, Manpreet S ^b   Mauermann, Michelle L ^b  

^a Mayo Clinic College of Medicine   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

LONG CHAIN ACYL COENZYME A DEHYDROGENASE; MITOCHONDRIAL TRIFUNCTIONAL PROTEIN;

CASE REPORT; COMPLICATION; DEFICIENCY; DISORDERS OF LIPID AND LIPOPROTEIN METABOLISM; HUMAN; MALE; MIDDLE AGED; RHABDOMYOLYSIS;

ACYL-COA DEHYDROGENASE, LONG-CHAIN; HUMANS; LIPID METABOLISM, INBORN ERRORS; MALE; MIDDLE AGED; MITOCHONDRIAL TRIFUNCTIONAL PROTEIN; RHABDOMYOLYSIS;

EID: 84892180227     PISSN: None     EISSN: 10974598     Source Type: Journal    
DOI: 10.1002/mus.23959     Document Type: Article

References (0)