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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

Detalles Bibliográficos
Autores principales: Salman, Mohd, Verma, Anshuman, Chaurasia, Sunita, Prasad, Deeksha, Kannabiran, Chitra, Singh, Vivek, Ramappa, Muralidhar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
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
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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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