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A Novel Mutation of CAPN1 Gene Causing Hereditary Spastic Paraplegia-76

Detalles Bibliográficos
Autores principales: Chinta, Vijayendra R., Krishnan, Pramod
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350748/
https://www.ncbi.nlm.nih.gov/pubmed/35936610
http://dx.doi.org/10.4103/aian.aian_977_21
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author Chinta, Vijayendra R.
Krishnan, Pramod
author_facet Chinta, Vijayendra R.
Krishnan, Pramod
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spelling pubmed-93507482022-08-05 A Novel Mutation of CAPN1 Gene Causing Hereditary Spastic Paraplegia-76 Chinta, Vijayendra R. Krishnan, Pramod Ann Indian Acad Neurol Letters to the Editor Wolters Kluwer - Medknow 2022 2022-05-03 /pmc/articles/PMC9350748/ /pubmed/35936610 http://dx.doi.org/10.4103/aian.aian_977_21 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
Chinta, Vijayendra R.
Krishnan, Pramod
A Novel Mutation of CAPN1 Gene Causing Hereditary Spastic Paraplegia-76
title A Novel Mutation of CAPN1 Gene Causing Hereditary Spastic Paraplegia-76
title_full A Novel Mutation of CAPN1 Gene Causing Hereditary Spastic Paraplegia-76
title_fullStr A Novel Mutation of CAPN1 Gene Causing Hereditary Spastic Paraplegia-76
title_full_unstemmed A Novel Mutation of CAPN1 Gene Causing Hereditary Spastic Paraplegia-76
title_short A Novel Mutation of CAPN1 Gene Causing Hereditary Spastic Paraplegia-76
title_sort novel mutation of capn1 gene causing hereditary spastic paraplegia-76
topic Letters to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350748/
https://www.ncbi.nlm.nih.gov/pubmed/35936610
http://dx.doi.org/10.4103/aian.aian_977_21
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