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Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9175893/ https://www.ncbi.nlm.nih.gov/pubmed/35844691 http://dx.doi.org/10.1002/jha2.267 |
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author | Waldstein, Sasha Arnold‐Croop, Sarah Carrel, Laura Eyster, M. Elaine |
author_facet | Waldstein, Sasha Arnold‐Croop, Sarah Carrel, Laura Eyster, M. Elaine |
author_sort | Waldstein, Sasha |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-9175893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91758932022-07-14 Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family Waldstein, Sasha Arnold‐Croop, Sarah Carrel, Laura Eyster, M. Elaine EJHaem Short Reports John Wiley and Sons Inc. 2021-07-22 /pmc/articles/PMC9175893/ /pubmed/35844691 http://dx.doi.org/10.1002/jha2.267 Text en © 2021 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Reports Waldstein, Sasha Arnold‐Croop, Sarah Carrel, Laura Eyster, M. Elaine Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family |
title | Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family |
title_full | Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family |
title_fullStr | Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family |
title_full_unstemmed | Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family |
title_short | Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family |
title_sort | diagnosing dehydrated hereditary stomatocytosis due to a kcnn4 gardos channel mutation: understanding challenges through study of a multi‐generational family |
topic | Short Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9175893/ https://www.ncbi.nlm.nih.gov/pubmed/35844691 http://dx.doi.org/10.1002/jha2.267 |
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