Multiple Acyl-CoA Dehydrogenase Deficiency: Phenotypic and Genetic Features of a Malaysian Cohort-Reference-Cited by-同舟云学术

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Multiple Acyl-CoA Dehydrogenase Deficiency: Phenotypic and Genetic Features of a Malaysian Cohort

Published:2024 Issue:4 Volume:20 Page:422
ISSN:1738-6586
Container-title:Journal of Clinical Neurology
language:en
Short-container-title:J Clin Neurol

Author:

Schee Jie Ping¹^ORCID,Tan Joo San²,Tan Cheng Yin¹^ORCID,Shahrizaila Nortina¹^ORCID,Wong Kum Thong²³^ORCID,Goh Khean Jin¹^ORCID

Affiliation:

1. Division of Neurology, Department of Medicine, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia.

2. Department of Pathology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia.

3. Jeffrey Cheah School of Medicine and Health Sciences, Monash University Malaysia, Selangor, Malaysia.

Funder

University of Malaya

Publisher

XMLink

Link

https://thejcn.com/pdf/10.3988/jcn.2023.0265

Reference30 articles.

1. Spectrum of metabolic myopathies

2. Metabolic myopathies: a guide and update for clinicians

3. ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency

4. Deficiency of electron transfer flavoprotein or electron transfer flavoprotein:ubiquinone oxidoreductase in glutaric acidemia type II fibroblasts.

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