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Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311843/ https://www.ncbi.nlm.nih.gov/pubmed/37386499 http://dx.doi.org/10.1186/s13023-023-02791-6 |
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author | Salman, Mohd Verma, Anshuman Chaurasia, Sunita Prasad, Deeksha Kannabiran, Chitra Singh, Vivek Ramappa, Muralidhar |
author_facet | Salman, Mohd Verma, Anshuman Chaurasia, Sunita Prasad, Deeksha Kannabiran, Chitra Singh, Vivek Ramappa, Muralidhar |
author_sort | Salman, Mohd |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-10311843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103118432023-07-01 Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy Salman, Mohd Verma, Anshuman Chaurasia, Sunita Prasad, Deeksha Kannabiran, Chitra Singh, Vivek Ramappa, Muralidhar Orphanet J Rare Dis Correction BioMed Central 2023-06-29 /pmc/articles/PMC10311843/ /pubmed/37386499 http://dx.doi.org/10.1186/s13023-023-02791-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Correction Salman, Mohd Verma, Anshuman Chaurasia, Sunita Prasad, Deeksha Kannabiran, Chitra Singh, Vivek Ramappa, Muralidhar Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy |
title | Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy |
title_full | Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy |
title_fullStr | Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy |
title_full_unstemmed | Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy |
title_short | Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy |
title_sort | correction to: identification and in silico analysis of a spectrum of slc4a11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy |
topic | Correction |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311843/ https://www.ncbi.nlm.nih.gov/pubmed/37386499 http://dx.doi.org/10.1186/s13023-023-02791-6 |
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