A Novel Mutation in the CLCN1 Gene Causing Autosomal Recessive Myotonia Congenita in Siblings

Detalles Bibliográficos
Autores principales: Chakravarty, Kamalesh, Lal, Vivek, Ray, Sucharita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Letters to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8513945/
https://www.ncbi.nlm.nih.gov/pubmed/34728966
http://dx.doi.org/10.4103/aian.AIAN_970_20
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author Chakravarty, Kamalesh
Lal, Vivek
Ray, Sucharita
author_facet Chakravarty, Kamalesh
Lal, Vivek
Ray, Sucharita
author_sort Chakravarty, Kamalesh
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spelling pubmed-85139452021-11-01 A Novel Mutation in the CLCN1 Gene Causing Autosomal Recessive Myotonia Congenita in Siblings Chakravarty, Kamalesh Lal, Vivek Ray, Sucharita Ann Indian Acad Neurol Letters to the Editor Wolters Kluwer - Medknow 2021 2021-05-28 /pmc/articles/PMC8513945/ /pubmed/34728966 http://dx.doi.org/10.4103/aian.AIAN_970_20 Text en Copyright: © 2006 - 2021 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
Chakravarty, Kamalesh
Lal, Vivek
Ray, Sucharita
A Novel Mutation in the CLCN1 Gene Causing Autosomal Recessive Myotonia Congenita in Siblings
title A Novel Mutation in the CLCN1 Gene Causing Autosomal Recessive Myotonia Congenita in Siblings
title_full A Novel Mutation in the CLCN1 Gene Causing Autosomal Recessive Myotonia Congenita in Siblings
title_fullStr A Novel Mutation in the CLCN1 Gene Causing Autosomal Recessive Myotonia Congenita in Siblings
title_full_unstemmed A Novel Mutation in the CLCN1 Gene Causing Autosomal Recessive Myotonia Congenita in Siblings
title_short A Novel Mutation in the CLCN1 Gene Causing Autosomal Recessive Myotonia Congenita in Siblings
title_sort novel mutation in the clcn1 gene causing autosomal recessive myotonia congenita in siblings
topic Letters to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8513945/
https://www.ncbi.nlm.nih.gov/pubmed/34728966
http://dx.doi.org/10.4103/aian.AIAN_970_20
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