Developmental study of α‐glucosidases in japanese quails with acid maltase deficiency

Muscle & Nerve

Volumn 9, Issue 6, 1986, Pages 537-543

  Usuki, Fusako ^a   Ishiura, Shoichi ^a   Sugita, Hideo ^a  

^a Natl Ctr Hosp Muscular Disorders   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLUCOSIDASE; GLUCAN 1,4 ALPHA GLUCOSIDASE;

ANIMAL EXPERIMENT; ANIMAL MODEL; EMBRYO; ENZYME DEFICIENCY; ETIOLOGY; HEREDITY; NONHUMAN; PRIORITY JOURNAL;

ALPHA-GLUCOSIDASES; ANIMAL; COTURNIX; EMBRYO; GLUCAN 1,4-ALPHA-GLUCOSIDASE; GLUCOSIDASES; GLYCOGEN; HYDROGEN-ION CONCENTRATION; ISOENZYMES; KINETICS; MUSCLES; NEUROMUSCULAR DISEASES; PECTORALIS MUSCLES; SUPPORT, NON-U.S. GOV'T; ZINC;

EID: 0022461297     PISSN: 0148639X     EISSN: 10974598     Source Type: Journal    
DOI: 10.1002/mus.880090610     Document Type: Article

References (13)

1. Comparative study of acid maltase deficiency
2. Genetic heterogeneity in acid α‐glucosidase deficiency
3. Adult‐onset acid maltase deficiency: a postmortem study
4. The spectrum and diagnosis of acid maltase deficiency
5. α‐Glucosidase deficiency in generalized glycogen storage disease (Pompe's disease)
6. Glycogen
7. Residual acid maltase activity in lateonset acid maltase deficiency
8. Type 2 glycogen storage disease in Japanese quails
9. Generalized glycogenosis in Brahman cattle
10. Bovine generalized glycogenosis
11. Biosynthesis of acid α‐glucosidase in late‐onset forms of glycogenosis type II (Pompe's disease)
12. Canine glycogen storage disease type II. A biochemical study of an acid α‐glucosidase deficient Lapland dog
13. Biochemical genetics of the Lapland dog model of glycogen storage disease type II (acid α‐glucosidase deficiency)