McArdle’s Disease

J Gordon Millichap

doi:10.15844/pedneurbriefs-2-11-10

McArdle’s Disease

Pediatric Neurology Briefs

Volume 2 (1988): Issue 11

By: J Gordon Millichap

Open Access

|Nov 1988

Abstract

Muscle biopsy specimens from 48 patients with biochemically proven phosphorylase deficiency (McArdle’s disease) have been analyzed by gel electrophoreis (SCS-PAGE), immunoblotting, and immunotitration (ELISA) at Columbia University College of Physicians and Surgeons, New York, NY.

References

Servidei S Shanske S Zeviani M Lebo R Fletterick R DiMauro S McArdle’s disease: biochemical and molecular genetic studies Ann Neurol 1988 Dec 24 6 774 81 10.1016/0887-8994(88)90072-0 3207360
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DOI: https://doi.org/10.15844/pedneurbriefs-2-11-10 | Journal eISSN: 2166-6482

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Language: English

Page range: 87 - 88

Published on: Nov 1, 1988

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Gel Electrophoreis,

Detectable Enzyme Protein,

Heterogeneity

© 1988 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 2 (1988): Issue 11