[Unusual phenotype of myopathy associated with a new PNPLA2 mutation]

Authors :: Guillemette, Jousserand
Nathalie, Streichenberger
Philippe, Petiot
Source :: Medecine sciences : M/S.
Publication Year :: 2016

Subjects :: Male
Muscle Cells
Biopsy
Lipase
Middle Aged
Immunohistochemistry
Lipids
Lipid Metabolism, Inborn Errors
Muscular Dystrophies
Phenotype
Muscular Diseases
Mutation
Humans
Cardiomyopathies

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