Skeletal Muscle Magnetic Resonance Imaging of the Lower Limbs in Late-onset Lipid Storage Myopathy with Electron Transfer Flavoprotein Dehydrogenase Gene Mutations-Reference-Cited by-同舟云学术

Skeletal Muscle Magnetic Resonance Imaging of the Lower Limbs in Late-onset Lipid Storage Myopathy with Electron Transfer Flavoprotein Dehydrogenase Gene Mutations

Published:2016-06-20 Issue:12 Volume:129 Page:1425-1431
ISSN:0366-6999
Container-title:Chinese Medical Journal
language:en
Short-container-title:

Author:

Liu Xin-Yi,Jin Ming,Wang Zhi-Qiang,Wang Dan-Ni,He Jun-Jie,Lin Min-Ting,Fu Hong-Xia,Wang Ning

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference24 articles.

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3. The electron transfer flavoprotein: Ubiquinone oxidoreductases;Watmough;Biochim Biophys Acta,2010

4. Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency;Xi;J Inherit Metab Dis,2014

5. Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in Southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A;Wang;J Mol Med (Berl,2011

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