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Muscle fiber-type distribution, fiber-type-specific damage, and the Pompe disease phenotype.
van den Berg, L E M; Drost, M R; Schaart, G; de Laat, J; van Doorn, P A; van der Ploeg, A T; Reuser, A J J.
Affiliation
  • van den Berg LE; Department of Pediatrics, Division of Metabolic Diseases and Genetics, Center for Lysosomal and Metabolic Diseases, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
J Inherit Metab Dis ; 36(5): 787-94, 2013 Sep.
Article in En | MEDLINE | ID: mdl-23053471
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glycogen Storage Disease Type II / Muscle Fibers, Skeletal Type of study: Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Adolescent / Adult / Humans Language: En Journal: J Inherit Metab Dis Year: 2013 Type: Article Affiliation country: Netherlands
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glycogen Storage Disease Type II / Muscle Fibers, Skeletal Type of study: Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Adolescent / Adult / Humans Language: En Journal: J Inherit Metab Dis Year: 2013 Type: Article Affiliation country: Netherlands