Genotype–phenotype correlation in children with hereditary spherocytosis-Reference-Cited by-同舟云学术

Genotype–phenotype correlation in children with hereditary spherocytosis

Published:2020-05-20 Issue:3 Volume:191 Page:486-496
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br. J. Haematol.

Author:

Tole Soumitra¹²³^ORCID,Dhir Priya⁴,Pugi Jakob¹,Drury Luke J.⁵,Butchart Sheila⁶,Fantauzzi Michelle⁶,Langer Jacob C.⁷,Baker Jillian M.¹⁴⁸,Blanchette Victor S.¹,Kirby‐Allen Melanie¹,Carcao Manuel D.¹⁹

Affiliation:

1. Department of Paediatrics Division of Haematology/Oncology Hospital for Sick Children Toronto OntarioCanada

2. Department of Paediatrics Division of Haematology/Oncology Children's HospitalLondon Health Sciences Centre London OntarioCanada

3. Western University London OntarioCanada

4. Faculty of Medicine University of Toronto Toronto Ontario Canada

5. PreventionGenetics Marshfield Wisconsin USA

6. Department of Nursing Hospital for Sick Children Toronto OntarioCanada

7. Department of Surgery Hospital for Sick Children and Department of Surgery University of Toronto Toronto OntarioCanada

8. Department of Pediatrics St. Michael's Hospital Toronto OntarioCanada

9. Child Health Evaluative Sciences, Research Institute Hospital for Sick Children Toronto Ontario Canada

Funder

Hospital for Sick Children

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.16750

Reference19 articles.

1. Hereditary spherocytosis

2. Ankyrin–1 mutations are a major cause of dominant and recessive hereditary spherocytosis

3. Hereditary spherocytosis—defects in proteins that connect the membrane skeleton to the lipid bilayer

4. Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency

5. Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population;Yawata Y;Int J Hematol,2000

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