Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency

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Detalles Bibliográficos
Autores principales: Chen, Hai-Zhu, Jin, Ming, Cai, Nai-Qing, Lin, Xiao-Dan, Liu, Xin-Yi, Xu, Liu-Qing, Lin, Min-Ting, Lin, Feng, Wang, Ning, Wang, Zhi-Qiang, Xu, Guo-Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Correspondence
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6616237/
https://www.ncbi.nlm.nih.gov/pubmed/31058673
http://dx.doi.org/10.1097/CM9.0000000000000288

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6616237/
https://www.ncbi.nlm.nih.gov/pubmed/31058673
http://dx.doi.org/10.1097/CM9.0000000000000288

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