Hereditary Spastic Paraplegia Type 35 with a Novel Mutation in Fatty Acid 2-Hydroxylase Gene and Literature Review of the Clinical Features

Detalles Bibliográficos
Autores principales: Incecik, Faruk, Besen, Seyda, Bozdogan, Sevcan Tug
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Letters to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238570/
https://www.ncbi.nlm.nih.gov/pubmed/30532373
http://dx.doi.org/10.4103/aian.AIAN_106_18
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author Incecik, Faruk
Besen, Seyda
Bozdogan, Sevcan Tug
author_facet Incecik, Faruk
Besen, Seyda
Bozdogan, Sevcan Tug
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spelling pubmed-62385702018-12-07 Hereditary Spastic Paraplegia Type 35 with a Novel Mutation in Fatty Acid 2-Hydroxylase Gene and Literature Review of the Clinical Features Incecik, Faruk Besen, Seyda Bozdogan, Sevcan Tug Ann Indian Acad Neurol Letters to the Editor Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6238570/ /pubmed/30532373 http://dx.doi.org/10.4103/aian.AIAN_106_18 Text en Copyright: © 2018 Annals of Indian Academy of Neurology http://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
Incecik, Faruk
Besen, Seyda
Bozdogan, Sevcan Tug
Hereditary Spastic Paraplegia Type 35 with a Novel Mutation in Fatty Acid 2-Hydroxylase Gene and Literature Review of the Clinical Features
title Hereditary Spastic Paraplegia Type 35 with a Novel Mutation in Fatty Acid 2-Hydroxylase Gene and Literature Review of the Clinical Features
title_full Hereditary Spastic Paraplegia Type 35 with a Novel Mutation in Fatty Acid 2-Hydroxylase Gene and Literature Review of the Clinical Features
title_fullStr Hereditary Spastic Paraplegia Type 35 with a Novel Mutation in Fatty Acid 2-Hydroxylase Gene and Literature Review of the Clinical Features
title_full_unstemmed Hereditary Spastic Paraplegia Type 35 with a Novel Mutation in Fatty Acid 2-Hydroxylase Gene and Literature Review of the Clinical Features
title_short Hereditary Spastic Paraplegia Type 35 with a Novel Mutation in Fatty Acid 2-Hydroxylase Gene and Literature Review of the Clinical Features
title_sort hereditary spastic paraplegia type 35 with a novel mutation in fatty acid 2-hydroxylase gene and literature review of the clinical features
topic Letters to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238570/
https://www.ncbi.nlm.nih.gov/pubmed/30532373
http://dx.doi.org/10.4103/aian.AIAN_106_18
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AT besenseyda hereditaryspasticparaplegiatype35withanovelmutationinfattyacid2hydroxylasegeneandliteraturereviewoftheclinicalfeatures
AT bozdogansevcantug hereditaryspasticparaplegiatype35withanovelmutationinfattyacid2hydroxylasegeneandliteraturereviewoftheclinicalfeatures

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