Molecular and functional characterisation of mild MCAD deficiency-Reference-Cited by-同舟云学术

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Molecular and functional characterisation of mild MCAD deficiency

Published:2001-05-22 Issue:5 Volume:108 Page:404-408
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

Zschocke Johannes,Schulze Andreas,Lindner Martin,Fiesel Sonja,Olgemöller Katharina,Hoffmann Georg,Penzien Johannes,Ruiter Jos,Wanders Ronald,Mayatepek Ertan

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s004390100501.pdf

Cited by 53 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Congenital disorders of glucose metabolism in adults with nondiabetic hypoglycemia;Obesity and metabolism;2024-06-17

2. Assessing the quality and value of metabolic chart data for capturing core outcomes for pediatric medium-chain acyl-CoA dehydrogenase (MCAD) deficiency;BMC Pediatrics;2024-01-13

3. Medium Chain Acyl CoA Dehydrogenase Deficiency and Eating Disorders: An Underreported Coincidence;Journal of Inborn Errors of Metabolism and Screening;2024

4. Free carnitine concentrations and biochemical parameters in medium‐chain acyl‐CoA dehydrogenase deficiency: Genotype–phenotype correlation;Clinical Genetics;2023-03-13

5. Interpreting phospholipid and cardiolipin profiles in rare mitochondrial diseases;Current Opinion in Systems Biology;2021-12

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