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CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8680880/ https://www.ncbi.nlm.nih.gov/pubmed/35002148 http://dx.doi.org/10.4103/aian.AIAN_1130_20 |
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author | Panda, Prateek K. Lourembam, Radhapyari Sharawat, Indar K. |
author_facet | Panda, Prateek K. Lourembam, Radhapyari Sharawat, Indar K. |
author_sort | Panda, Prateek K. |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-8680880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-86808802022-01-06 CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders Panda, Prateek K. Lourembam, Radhapyari Sharawat, Indar K. Ann Indian Acad Neurol Letters to the Editor Wolters Kluwer - Medknow 2021 2021-02-04 /pmc/articles/PMC8680880/ /pubmed/35002148 http://dx.doi.org/10.4103/aian.AIAN_1130_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 Panda, Prateek K. Lourembam, Radhapyari Sharawat, Indar K. CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders |
title | CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders |
title_full | CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders |
title_fullStr | CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders |
title_full_unstemmed | CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders |
title_short | CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders |
title_sort | cnnm2 heterozygous variant presenting as hypomagnesemia and west syndrome: expanding the spectrum of cnnm2 gene-related epileptic disorders |
topic | Letters to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8680880/ https://www.ncbi.nlm.nih.gov/pubmed/35002148 http://dx.doi.org/10.4103/aian.AIAN_1130_20 |
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