Familial pseudohyperkalemia in blood donors: a novel mutation with implications for transfusion practice-Reference-Cited by-同舟云学术

Familial pseudohyperkalemia in blood donors: a novel mutation with implications for transfusion practice

Published:2014-06-19 Issue:12 Volume:54 Page:3043-3050
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Bawazir Waleed M.¹²,Flatt Joanna F.¹,Wallis Jonathan P.³,Rendon Augusto⁴,Cardigan Rebecca A.⁵,New Helen V.⁶,Wiltshire Michael⁵,Page Lizanne⁷,Chapman Catherine E.⁸,Stewart Gordon W.⁹,Bruce Lesley J.¹

Affiliation:

1. Bristol Institute for Transfusion Sciences; NHS Blood & Transplant; Bristol UK

2. School of Biochemistry; University of Bristol; Bristol UK

3. Newcastle upon Tyne Hospitals NHS Foundation Trust; Newcastle upon Tyne UK

4. Department of Haematology; University of Cambridge, NHS Blood & Transplant, & NIHR Biomedical Research Centre; Cambridge UK

5. Components Development Laboratory; NHS Blood & Transplant; Brentwood UK

6. Imperial College Healthcare NHS Trust/NHS Blood & Transplant; London UK

7. NHS Blood & Transplant Colindale Centre; London UK

8. NHS Blood & Transplant Newcastle Centre; Newcastle upon Tyne UK

9. School of Life and Medical Sciences; University College London; London UK

Funder

King Abdulaziz University, Faculty of Applied Medical Sciences, Jeddah, Saudi Arabia

UK National Health Service R & D Directorate

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/trf.12757/fullpdf

Reference25 articles.

1. Red cell changes during storage;Hess;Transfus Apher Sci,2010

2. Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1;Bruce;Nat Genet,2005

3. The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein;Bruce;Blood,2009

4. Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome;Flatt;Blood,2011

5. Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis;Zarychanski;Blood,2012

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