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Hereditary anemia caused by multilocus inheritance of PIEZO1, SLC4A1 and ABCB6 mutations: a diagnostic and therapeutic challenge
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Fondazione Ferrata Storti
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9425304/ https://www.ncbi.nlm.nih.gov/pubmed/35443567 http://dx.doi.org/10.3324/haematol.2022.280799 |
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author | Rosato, Barbara Eleni Alper, Seth L. Tomaiuolo, Giovanna Russo, Roberta Iolascon, Achille Andolfo, Immacolata |
author_facet | Rosato, Barbara Eleni Alper, Seth L. Tomaiuolo, Giovanna Russo, Roberta Iolascon, Achille Andolfo, Immacolata |
author_sort | Rosato, Barbara Eleni |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-9425304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Fondazione Ferrata Storti |
record_format | MEDLINE/PubMed |
spelling | pubmed-94253042022-09-15 Hereditary anemia caused by multilocus inheritance of PIEZO1, SLC4A1 and ABCB6 mutations: a diagnostic and therapeutic challenge Rosato, Barbara Eleni Alper, Seth L. Tomaiuolo, Giovanna Russo, Roberta Iolascon, Achille Andolfo, Immacolata Haematologica Case Report Fondazione Ferrata Storti 2022-04-21 /pmc/articles/PMC9425304/ /pubmed/35443567 http://dx.doi.org/10.3324/haematol.2022.280799 Text en Copyright© 2022 Ferrata Storti Foundation https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Case Report Rosato, Barbara Eleni Alper, Seth L. Tomaiuolo, Giovanna Russo, Roberta Iolascon, Achille Andolfo, Immacolata Hereditary anemia caused by multilocus inheritance of PIEZO1, SLC4A1 and ABCB6 mutations: a diagnostic and therapeutic challenge |
title | Hereditary anemia caused by multilocus inheritance of PIEZO1, SLC4A1 and ABCB6 mutations: a diagnostic and therapeutic challenge |
title_full | Hereditary anemia caused by multilocus inheritance of PIEZO1, SLC4A1 and ABCB6 mutations: a diagnostic and therapeutic challenge |
title_fullStr | Hereditary anemia caused by multilocus inheritance of PIEZO1, SLC4A1 and ABCB6 mutations: a diagnostic and therapeutic challenge |
title_full_unstemmed | Hereditary anemia caused by multilocus inheritance of PIEZO1, SLC4A1 and ABCB6 mutations: a diagnostic and therapeutic challenge |
title_short | Hereditary anemia caused by multilocus inheritance of PIEZO1, SLC4A1 and ABCB6 mutations: a diagnostic and therapeutic challenge |
title_sort | hereditary anemia caused by multilocus inheritance of piezo1, slc4a1 and abcb6 mutations: a diagnostic and therapeutic challenge |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9425304/ https://www.ncbi.nlm.nih.gov/pubmed/35443567 http://dx.doi.org/10.3324/haematol.2022.280799 |
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