Phospholipid composition of cultivated skin fibroblasts in Duchenne's muscular dystrophy
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference8 articles.
1. Evidence for the release of enzymes from different organs in Duchenne's muscular dystrophy
2. Erythrocyte Deformation in Human Muscular Dystrophy
3. Erythrozytenlipide bei progressiver muskeldystrophie
4. Der einbau von [14C] fettsäuren in muskellipide bei progressiver muskeldystrophie (duchenne)
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1. Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders;Journal of Lipid Research;2012-01
2. Phospholipid mass is increased in fibroblasts bearing the Swedish amyloid precursor mutation;Brain Research Bulletin;2006-03
3. Phospholipid composition and levels are not altered in fibroblasts bearing presenilin-1 mutations;Brain Research Bulletin;2000-06
4. Molecular Genetics of Duchenne and Becker Muscular Dystrophy;International Review of Neurobiology;1988
5. Inherited Membrane Disorders of Muscle;Clinical Disorders of Membrane Transport Processes;1987
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