Overhydrated hereditary stomatocytosis: A rare cause of familiar persistent macrocytosis due to <i>SLC4A1</i> variants-Reference-Cited by-同舟云学术

Overhydrated hereditary stomatocytosis: A rare cause of familiar persistent macrocytosis due to SLC4A1 variants

Published:2023-04-14 Issue:9 Volume:70 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Marcello Anna Paola¹^ORCID,Visconti Camilla²³,Vercellati Cristina¹,Zaninoni Anna¹,Bianchi Paola¹^ORCID,Barcellini Wilma¹,Aiuti Alessandro²³,Fermo Elisa¹,Ferrua Francesca²

Affiliation:

1. Hematology Unit Pathophysiology of Anemias Unit Foundation IRCCS Ca’ Granda Ospedale Maggiore Policlinico Milan Italy

2. Pediatric Immunohematology and Bone Marrow Transplantation Unit San Raffaele Telethon Institute for Gene Therapy (SR‐Tiget) IRCCS San Raffaele Scientific Institute Milan Italy

3. Department of Pediatrics Vita‐Salute San Raffaele University Milan Italy

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.30344

Reference17 articles.

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3. Band 3, the human red cell chloride/bicarbonate anion exchanger (AE1, SLC4A1), in a structural context

4. Hereditary stomatocytosis and cation leaky red cells — Recent developments

5. The mechanosensitive Piezo1 channel: structural features and molecular bases underlying its ion permeation and mechanotransduction

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1. Transient presence of stomatocytes: A clue to the diagnosis of overhydrated hereditary stomatocytosis in a child with beta‐thalassemia;Journal of Clinical Laboratory Analysis;2023-12

2. An erythrocyte-centric view on the MFSD2B sphingosine-1-phosphate transporter;Pharmacology & Therapeutics;2023-09