Novel ETFDH mutations in four cases of riboflavin responsive multiple acyl-CoA dehydrogenase deficiency

Multiple acyl-CoA dehydrogenase deficiency (MADD) is an autosomal recessive disorder of fatty acid, amino acid, and choline metabolism caused by mutations in EFTA, EFTB, or ETFDH. Many MADD patients are responsive to treatment with riboflavin, termed riboflavin-responsive MADD (RR-MADD). Here, we re...

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Detalles Bibliográficos
Autores principales: Fan, Xin, Xie, Bobo, Zou, Jun, Luo, Jingsi, Qin, Zailong, D'Gama, Alissa M., Shi, Jiahai, Yi, Shang, Yang, Qi, Wang, Jin, Luo, Shiyu, Chen, Shaoke, Agrawal, Pankaj B., Li, Qifei, Shen, Yiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031868/
https://www.ncbi.nlm.nih.gov/pubmed/29988809
http://dx.doi.org/10.1016/j.ymgmr.2018.05.007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031868/
https://www.ncbi.nlm.nih.gov/pubmed/29988809
http://dx.doi.org/10.1016/j.ymgmr.2018.05.007

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