An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

Journal of the Neurological Sciences

Volumn 62, Issue 1-3, 1983, Pages 327-355

  Barth, P G ^a,b   Scholte, H R ^c   Berden, J A ^d   Van Der Klei Van Moorsel, J M ^a   Luyt Houwen, I E M ^c   Van'T Veer Korthof, E Th ^e   Van Der Harten, J J ^b   Sobotka Plojhar, M A ^a  

^a Department of Pediatrics Divisions of Pediatric Neurology Research Biochemistry and Pediatric Cardiology ^*  (Netherlands)

^b VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^c ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

^d UNIVERSITY OF AMSTERDAM   (Netherlands)

^e LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Cardiomyopathy; Carnitine; Lactic acidemia; Mitochondria; Neuromuscular disease; Neutrophil leucocytes; X linkage

Indexed keywords

ADENOSINE PHOSPHATE DEAMINASE; ADENOSINE TRIPHOSPHATASE; CYTOCHROME; ADENOSINE TRIPHOSPHATASE (CALCIUM MAGNESIUM); CA(2+) MG(2+) ATPASE; CARNITINE;

AUTOPSY; BLOOD AND HEMOPOIETIC SYSTEM; CARDIOMYOPATHY; CHILD; CLINICAL ARTICLE; HEART; HEREDITY; HISTOLOGY; HUMAN; MITOCHONDRIAL MYOPATHY; MUSCLE; NEUTROPENIA; X CHROMOSOME RECESSIVE INHERITANCE; ADULT; AGED; ARTICLE; BLOOD; CASE REPORT; DIET THERAPY; FEMALE; GENETIC LINKAGE; GENETICS; HETEROZYGOTE DETECTION; MALE; METABOLISM; MUSCLE MITOCHONDRION; MYOCARDIAL DISEASE; NEUTROPHIL; OXIDATIVE PHOSPHORYLATION; PATHOLOGY; PATHOPHYSIOLOGY; PEDIGREE; PHYSIOLOGY; SYNDROME; X CHROMOSOME;

ADENOSINETRIPHOSPHATASE; ADULT; AGED; CA(2+) MG(2+)-ATPASE; CARNITINE; CASE REPORT; CYTOCHROMES; FEMALE; HETEROZYGOTE DETECTION; HUMAN; LINKAGE (GENETICS); MALE; MIDDLE AGE; MITOCHONDRIA, MUSCLE; MUSCLES; MYOCARDIAL DISEASES; NEUTROPHILS; OXIDATIVE PHOSPHORYLATION; PEDIGREE; SYNDROME; X CHROMOSOME;

EID: 0020974404     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0022-510X(83)90209-5     Document Type: Article

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