Lipid Storage Myopathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,General Neuroscience
Link
http://link.springer.com/content/pdf/10.1007/s11910-010-0154-y.pdf
Reference38 articles.
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3. Vermeire S, Rutgeerts P: Current status of genetics research in inflammatory bowel disease. Genes Immun 2005, 6:637–645.
4. Yamak AA, Bitar F, Karam P, et al.: Exclusive cardiac dysfunction in familial primary carnitine deficiency cases: a genotype-phenotype correlation. Clin Genet 2007, 72:59–62.
5. Wang Y, Korman SH, Ye J, et al.: Phenotype and genotype variation in primary carnitine deficiency. Genet Med 2001, 3:387–392.
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