P1537: HEREDITARY ANEMIA CAUSED BY MULTILOCUS INHERITANCE OF PIEZO1, SLC4A1 AND ABCB6 MUTATIONS: A DIAGNOSTIC AND THERAPEUTIC CHALLENGE.

Detalles Bibliográficos
Autores principales: Rosato, B. E., Alper, S. L., Tomaiuolo, G., Russo, R., Iolascon, A., Andolfo, I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Posters
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9430513/
http://dx.doi.org/10.1097/01.HS9.0000849004.04269.ae
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author Rosato, B. E.
Alper, S. L.
Tomaiuolo, G.
Russo, R.
Iolascon, A.
Andolfo, I.
author_facet Rosato, B. E.
Alper, S. L.
Tomaiuolo, G.
Russo, R.
Iolascon, A.
Andolfo, I.
author_sort Rosato, B. E.
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spelling pubmed-94305132022-08-31 P1537: HEREDITARY ANEMIA CAUSED BY MULTILOCUS INHERITANCE OF PIEZO1, SLC4A1 AND ABCB6 MUTATIONS: A DIAGNOSTIC AND THERAPEUTIC CHALLENGE. Rosato, B. E. Alper, S. L. Tomaiuolo, G. Russo, R. Iolascon, A. Andolfo, I. Hemasphere Posters Lippincott Williams & Wilkins 2022-06-23 /pmc/articles/PMC9430513/ http://dx.doi.org/10.1097/01.HS9.0000849004.04269.ae Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access Abstract Book distributed under the Attribution-NonCommercial-NoDerivs (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) which allows third parties to download the articles and share them with others as long as they credit the author and the Abstract Book, but they cannot change the content in any way or use them commercially.
spellingShingle Posters
Rosato, B. E.
Alper, S. L.
Tomaiuolo, G.
Russo, R.
Iolascon, A.
Andolfo, I.
P1537: HEREDITARY ANEMIA CAUSED BY MULTILOCUS INHERITANCE OF PIEZO1, SLC4A1 AND ABCB6 MUTATIONS: A DIAGNOSTIC AND THERAPEUTIC CHALLENGE.
title P1537: HEREDITARY ANEMIA CAUSED BY MULTILOCUS INHERITANCE OF PIEZO1, SLC4A1 AND ABCB6 MUTATIONS: A DIAGNOSTIC AND THERAPEUTIC CHALLENGE.
title_full P1537: HEREDITARY ANEMIA CAUSED BY MULTILOCUS INHERITANCE OF PIEZO1, SLC4A1 AND ABCB6 MUTATIONS: A DIAGNOSTIC AND THERAPEUTIC CHALLENGE.
title_fullStr P1537: HEREDITARY ANEMIA CAUSED BY MULTILOCUS INHERITANCE OF PIEZO1, SLC4A1 AND ABCB6 MUTATIONS: A DIAGNOSTIC AND THERAPEUTIC CHALLENGE.
title_full_unstemmed P1537: HEREDITARY ANEMIA CAUSED BY MULTILOCUS INHERITANCE OF PIEZO1, SLC4A1 AND ABCB6 MUTATIONS: A DIAGNOSTIC AND THERAPEUTIC CHALLENGE.
title_short P1537: HEREDITARY ANEMIA CAUSED BY MULTILOCUS INHERITANCE OF PIEZO1, SLC4A1 AND ABCB6 MUTATIONS: A DIAGNOSTIC AND THERAPEUTIC CHALLENGE.
title_sort p1537: hereditary anemia caused by multilocus inheritance of piezo1, slc4a1 and abcb6 mutations: a diagnostic and therapeutic challenge.
topic Posters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9430513/
http://dx.doi.org/10.1097/01.HS9.0000849004.04269.ae
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