Dominantly inherited cardioskeletal myopathy with lysosomal glycogen storage and normal acid maltase levels

Byrne, E; Dennett, X; Crotty, Brendan; Trounce, I; Sands, JM; Hawkins, R; Hammond, J; Anderson, S; Haan, EA; Pollard, A

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Dominantly inherited cardioskeletal myopathy with lysosomal glycogen storage and normal acid maltase levels

Version 2 2024-06-03, 10:41

Version 1 2022-11-29, 23:23

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posted on 2024-06-03, 10:41 authored by E Byrne, X Dennett, Brendan CrottyBrendan Crotty, I Trounce, JM Sands, R Hawkins, J Hammond, S Anderson, EA Haan, A Pollard

Dominantly inherited cardioskeletal myopathy with lysosomal glycogen storage and normal acid maltase levels

History

Journal

Brain

Volume

109

Pagination

523-536

Location

England

Publisher DOI

https://doi.org/10.1093/brain/109.3.523

ISSN

0006-8950

eISSN

1460-2156

Language

en

Publication classification

C1.1 Refereed article in a scholarly journal

Issue

3

Publisher

Oxford University Press (OUP)

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Keywords

Adult Cardiomyopathies Cardiomyopathy, Dilated Glucan 1,4-alpha-Glucosidase Glucosidases Glycogen Storage Disease Humans Male Metabolism, Inborn Errors Pedigree Syndrome

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Dominantly inherited cardioskeletal myopathy with lysosomal glycogen storage and normal acid maltase levels

History

Journal

Volume

Pagination

Location

Publisher DOI

ISSN

eISSN

Language

Publication classification

Issue

Publisher

Usage metrics

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Keywords

Licence

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