Adult polyglucosan body disease: Case description of an expanding genetic and clinical syndrome

Author:

Klein Christopher J.,Boes Christopher J.,Chapin John E.,Lynch Christopher D.,Campeau Norbert G.,Dyck P. James B.,Dyck Peter J.

Funder

The Mayo Foundation, Rochester, Minnesota

Mayo Gene Discovery Shared Resource (Mayo Comprehensive Cancer Center Grant) from the National Cancer Institute

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Reference19 articles.

1. Muscle phosphofructokinase deficiency: tow cases with unusual polysaccharide accumulation and immunologically active enzyme protein;Agamanolis;Muscle Nerve,1980

2. Extensive white-matter changes in case of adult polyglucosan body disease;Berkhoff;Neuroradiology,2001

3. Familial dementia due to adult polyglucosan body disease;Bigio;Clin Neuropathol,1997

4. Branching enzyme activity of cultured amniocytes and chorionic villi: prenatal testing for type IV glycogen storage disease;Brown;Am J Hum Genet,1989

5. Lack of an alpha-1,4-glucan: alpha-1,4-glucan 6-glycosyl transferase in a case of type IV glycogenosis;Brown;Proc Natl Acad Sci USA,1966

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