Severe hemolytic anemia in a newborn: Look out for rare Gardos channelopathies due to KCNN4 mutation-Reference-Cited by-同舟云学术

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Severe hemolytic anemia in a newborn: Look out for rare Gardos channelopathies due to KCNN4 mutation

Published:2023-05-02 Issue:8 Volume:70 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Munaretto Vania¹,Martella Maddalena¹,Francescato Samuela¹,Reggiani Giulia¹,Boaro Maria Paola¹,Bianchi Paola²^ORCID,Fermo Elisa²,Barcellini Wilma²,Sainati Laura¹,Colombatti Raffaella¹

Affiliation:

1. Onco‐Ematologia Pediatrica Dipartimento di Salute della Donna e del Bambino Azienda Ospedaliera‐Università di Padova Padua Italy

2. UOC Ematologia UOS Fisiopatologia delle anemie Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico Milan Italy

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.30325

Reference12 articles.

1. Anemia and transfusion in the neonate

2. A New Variant of Hereditary Hemolytic Anemia With Stomatocytosis and Erythrocyte Cation Abnormality

3. Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis

4. The Gárdos channel: a review of the Ca2+-activated K+ channel in human erythrocytes

5. Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis)

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