Dystrophin in Limb-Girdle Dystrophy

J Gordon Millichap

doi:10.15844/pedneurbriefs-5-11-3

Dystrophin in Limb-Girdle Dystrophy

Pediatric Neurology Briefs

Volume 5 (1991): Issue 11

By: J Gordon Millichap

Open Access

|Nov 1991

Abstract

Dystrophin content in muscle was analyzed by both immunofluorescence and immunoblot in 41 patients with a clinical diagnosis of limb-girdle muscular dystrophy seen at the National Institute of Neuroscience, Tokyo, Japan over a 12-year period.

References

Arikawa E Hoffman EP Kaido M Nonaka I Sugita H Arahata K The frequency of patients with dystrophin abnormalities in a limb-girdle patient population Neurology 1991 Sep 41 9 1491 1496 10.1212/WNL.41.9.1491 1842672
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Hoffman EP Garcia CA Chamberlain JS Angelini C Lupski JR Fenwick R Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of Duchenne muscular dystrophy Ann Neurol 1991 Oct 30 4 605 610 10.1002/ana.410300414 1789686
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Matsumura K Toda T Hasegawa T Kamei M Imoto N Shimizu T A Japanese family with two types of muscular dystrophy: DNA analysis and the dystrophin test J Child Neurol 1991 Jul 6 3 251 256 10.1177/088307389100600309 1875028
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-5-11-3 | Journal eISSN: 2166-6482

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Language: English

Page range: 82 - 83

Published on: Nov 1, 1991

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Dystrophin,

Limb-Girdle Muscular Dystrophy,

Carboxyl-Terminus

© 1991 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 5 (1991): Issue 11