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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:
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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author Korula, Sophy
Yoganathan, Sangeetha
Peter, Jeyanthi
Chandran, Mahalakshmi
Christudass, Chrithunesa S.
Danda, Sumita
author_facet Korula, Sophy
Yoganathan, Sangeetha
Peter, Jeyanthi
Chandran, Mahalakshmi
Christudass, Chrithunesa S.
Danda, Sumita
author_sort Korula, Sophy
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spelling pubmed-97648792022-12-21 Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Treatable Neurometabolic Disorder Korula, Sophy Yoganathan, Sangeetha Peter, Jeyanthi Chandran, Mahalakshmi Christudass, Chrithunesa S. Danda, Sumita Ann Indian Acad Neurol Letters to the Editor Wolters Kluwer - Medknow 2022 2022-10-31 /pmc/articles/PMC9764879/ /pubmed/36561017 http://dx.doi.org/10.4103/aian.aian_370_22 Text en Copyright: © 2022 Annals of Indian Academy of Neurology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Letters to the Editor
Korula, Sophy
Yoganathan, Sangeetha
Peter, Jeyanthi
Chandran, Mahalakshmi
Christudass, Chrithunesa S.
Danda, Sumita
Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Treatable Neurometabolic Disorder
title Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Treatable Neurometabolic Disorder
title_full Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Treatable Neurometabolic Disorder
title_fullStr Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Treatable Neurometabolic Disorder
title_full_unstemmed Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Treatable Neurometabolic Disorder
title_short Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Treatable Neurometabolic Disorder
title_sort late onset multiple acyl-coa dehydrogenase deficiency: a rare treatable neurometabolic disorder
topic Letters to the Editor
url 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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