Glycogen pathways in disease: new developments in a classical field of medical genetics

Journal of Inherited Metabolic Disease

Volumn 38, Issue 3, 2015, Pages 483-487

  Kilimann, Manfred W ^a,b   Oldfors, Anders ^c  

^a UNIVERSITY MEDICAL CENTER GÖTTINGEN   (Germany)

^b MAX PLANCK INSTITUTE OF EXPERIMENTAL MEDICINE   (Germany)

^c UNIVERSITY OF GOTHENBURG   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOGEN;

ANIMAL; GENETICS; GLYCOGEN STORAGE DISEASE; GLYCOLYSIS; HUMAN; MEDICAL GENETICS; MUSCLE; PATHOLOGY;

ANIMALS; GENETICS, MEDICAL; GLYCOGEN; GLYCOGEN STORAGE DISEASE; GLYCOLYSIS; HUMANS; MUSCLES;

EID: 84939962655     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-014-9785-5     Document Type: Article

References (2)

1. Chen YT (2000) Glycogen storage diseases. In Scriver CR, Beaudet AL, Valle D, Sly WS, Childs B, Kinzler KW, Vogelstein B, eds. Metabolic and molecular basis of inherited disease, Chapt 71 (8th edn). New York: McGraw-Hill, 1521–1552
2. Hirschhorn R, Reuser AJJ (2000) GSD type II: acid a-glucosidase (acid maltase) deficiency. In Scriver CR, Beaudet AL, Valle D, Sly WS, Childs B, Kinzler KW, Vogelstein B, eds. Metabolic and molecular basis of inherited disease, Chapt 135 (8th edn). New York: McGraw-Hill, 3389–3420