Mitochondrial changes in muscle phosphoglycerate kinase deficiency

Clinical Neuropathology

Volumn 15, Issue 1, 1996, Pages 34-40

  Schroder J M ^a   Dodel, R ^a   Weis, J ^a   Stefanidis, I ^a   Reichmann, H ^b  

^a RWTH AACHEN UNIVERSITY   (Germany)

^b UNIVERSITY OF WÜRZBURG   (Germany)

Author keywords

Mitochondria; Myopathy; Phosphoglycerate kinase; Type IX glycogenosis

Indexed keywords

PHOSPHOGLYCERATE KINASE;

ADULT; ARTICLE; CASE REPORT; ENZYME DEFICIENCY; GLYCOGEN STORAGE DISEASE; GLYCOGEN STORAGE DISEASE TYPE 9; HISTOCHEMISTRY; HUMAN; HUMAN TISSUE; MALE; MITOCHONDRION; MUSCLE BIOPSY; MYOPATHY; PRIORITY JOURNAL; ULTRASTRUCTURE;

ADULT; BIOPSY; ENDOTHELIUM; HUMANS; KIDNEY; LINKAGE (GENETICS); MALE; MITOCHONDRIA, MUSCLE; MUSCLE FIBERS; NERVE FIBERS; PHOSPHOGLYCERATE KINASE; X CHROMOSOME;

EID: 0030044866     PISSN: 07225091     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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