Neutral lipid storage disease with subclinical myopathy due to a retrotransposal insertion in the PNPLA2 gene-Reference-Cited by-同舟云学术

Neutral lipid storage disease with subclinical myopathy due to a retrotransposal insertion in the PNPLA2 gene

Published:2010-06 Issue:6 Volume:20 Page:397-402
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Akman Hasan O.,Davidzon Guido,Tanji Kurenai,MacDermott Emma J.,Larsen Louann,Davidson Mercy M.,Haller Ronald G.,Szczepaniak Lidia S.,Lehman Thomas J.A.,Hirano Michio,DiMauro Salvatore

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference26 articles.

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5. The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene;Gempel;Brain,2007

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