Type IV glycogen storage disease: Branching enzyme deficiency in skin fibroblasts and possible heterozygote detection

Author:

Howell R. Rodney,Kaback Michael M.,Brown Barbara I.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference9 articles.

1. Howell, R. R.: The glycogen storage diseases, Stanbury, J. B., Wyngaarden, J. B., and Frederickson, D. S., editors: in The metabolic basis of inherited disease, ed. 3, New York, McGraw-Hill Book Company. In press.

2. Type IV glycogenosis. Report of a case proven by characterization of glycogen and studied at necropsy;Sidbury;Bull. Hopkins Hosp.,1962

3. Structure of glycogens and amylopectins. III. Normal and abnormal human glycogens;Illingworth;J. Biol. Chem.,1952

4. Familial cirrhosis of the liver with storage of abnormal glycogen;Andersen;Lab. Invest.,1956

5. Lack of an α-1,4 glucan: α-1,4 glucan 6-glucosyltransferase in a case of type IV glycogenosis;Brown;Proc. Nat. Acad. Sci.,1966

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