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P1472: COINHERITANCE OF PIEZO1 VARIANTS AND MULTI-LOCUS RED BLOOD CELL DEFECTS ACCOUNT FOR THE SYMPTOMATIC PHENOTYPE IN BETA-THALASSEMIA CARRIERS.

Detalles Bibliográficos
Autores principales: Maria Pinto, Valeria, Russo, Roberta, Quintino, Sabrina, Eleni Rosato, Barbara, Marra, Roberta, Del Giudice, Federica, Mogni, Massimo, Maffei, Massimo, Iolascon, Achille, Luca Forni, Gian, Andolfo, Immacolata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10430197/
http://dx.doi.org/10.1097/01.HS9.0000972772.85628.08
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author Maria Pinto, Valeria
Russo, Roberta
Quintino, Sabrina
Eleni Rosato, Barbara
Marra, Roberta
Del Giudice, Federica
Mogni, Massimo
Maffei, Massimo
Iolascon, Achille
Luca Forni, Gian
Andolfo, Immacolata
author_facet Maria Pinto, Valeria
Russo, Roberta
Quintino, Sabrina
Eleni Rosato, Barbara
Marra, Roberta
Del Giudice, Federica
Mogni, Massimo
Maffei, Massimo
Iolascon, Achille
Luca Forni, Gian
Andolfo, Immacolata
author_sort Maria Pinto, Valeria
collection PubMed
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spelling pubmed-104301972023-08-17 P1472: COINHERITANCE OF PIEZO1 VARIANTS AND MULTI-LOCUS RED BLOOD CELL DEFECTS ACCOUNT FOR THE SYMPTOMATIC PHENOTYPE IN BETA-THALASSEMIA CARRIERS. Maria Pinto, Valeria Russo, Roberta Quintino, Sabrina Eleni Rosato, Barbara Marra, Roberta Del Giudice, Federica Mogni, Massimo Maffei, Massimo Iolascon, Achille Luca Forni, Gian Andolfo, Immacolata Hemasphere Posters Lippincott Williams & Wilkins 2023-08-08 /pmc/articles/PMC10430197/ http://dx.doi.org/10.1097/01.HS9.0000972772.85628.08 Text en Copyright © 2023 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
Maria Pinto, Valeria
Russo, Roberta
Quintino, Sabrina
Eleni Rosato, Barbara
Marra, Roberta
Del Giudice, Federica
Mogni, Massimo
Maffei, Massimo
Iolascon, Achille
Luca Forni, Gian
Andolfo, Immacolata
P1472: COINHERITANCE OF PIEZO1 VARIANTS AND MULTI-LOCUS RED BLOOD CELL DEFECTS ACCOUNT FOR THE SYMPTOMATIC PHENOTYPE IN BETA-THALASSEMIA CARRIERS.
title P1472: COINHERITANCE OF PIEZO1 VARIANTS AND MULTI-LOCUS RED BLOOD CELL DEFECTS ACCOUNT FOR THE SYMPTOMATIC PHENOTYPE IN BETA-THALASSEMIA CARRIERS.
title_full P1472: COINHERITANCE OF PIEZO1 VARIANTS AND MULTI-LOCUS RED BLOOD CELL DEFECTS ACCOUNT FOR THE SYMPTOMATIC PHENOTYPE IN BETA-THALASSEMIA CARRIERS.
title_fullStr P1472: COINHERITANCE OF PIEZO1 VARIANTS AND MULTI-LOCUS RED BLOOD CELL DEFECTS ACCOUNT FOR THE SYMPTOMATIC PHENOTYPE IN BETA-THALASSEMIA CARRIERS.
title_full_unstemmed P1472: COINHERITANCE OF PIEZO1 VARIANTS AND MULTI-LOCUS RED BLOOD CELL DEFECTS ACCOUNT FOR THE SYMPTOMATIC PHENOTYPE IN BETA-THALASSEMIA CARRIERS.
title_short P1472: COINHERITANCE OF PIEZO1 VARIANTS AND MULTI-LOCUS RED BLOOD CELL DEFECTS ACCOUNT FOR THE SYMPTOMATIC PHENOTYPE IN BETA-THALASSEMIA CARRIERS.
title_sort p1472: coinheritance of piezo1 variants and multi-locus red blood cell defects account for the symptomatic phenotype in beta-thalassemia carriers.
topic Posters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10430197/
http://dx.doi.org/10.1097/01.HS9.0000972772.85628.08
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