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Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Treatable Neurometabolic Disorder

Detalles Bibliográficos
Autores principales:	Korula, Sophy, Yoganathan, Sangeetha, Peter, Jeyanthi, Chandran, Mahalakshmi, Christudass, Chrithunesa S., Danda, Sumita
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer - Medknow 2022
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764879/ https://www.ncbi.nlm.nih.gov/pubmed/36561017 http://dx.doi.org/10.4103/aian.aian_370_22

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