Dominant inherited β‐thalassemia intermedia in a Polish family due to a novel frameshift mutation in <i>HBB</i>-Reference-Cited by-同舟云学术

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Dominant inherited β‐thalassemia intermedia in a Polish family due to a novel frameshift mutation in HBB

Published:2023-06-23 Issue:10 Volume:70 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Novak Wolfgang¹^ORCID,Sunder‐Plassmann Raute²,Berner Jakob¹³,Köhrer Stefan¹³,Zeitlhofer Petra³⁴,Haas Oskar A.¹⁴,Riedl Julia⁵,Kager Leo¹³,Sillaber Christian⁵

Affiliation:

1. Department of Pediatrics and Adolescent Medicine St. Anna Children's Hospital Medical University Vienna Vienna Austria

2. Department of Laboratory Medicine Medical University of Vienna Vienna Austria

3. St. Anna Children's Cancer Research Institute Vienna Austria

4. Labdia Labordiagnostik Vienna Austria

5. Division of Hematology Department of Internal Medicine Medical University of Vienna Vienna Austria

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.30511

Reference12 articles.

1. Inclusion-Body β-Thalassemia Trait

2. Molecular basis for dominantly inherited inclusion body beta-thalassemia.

3. β-thalassemia alleles and unstable hemoglobin types among russian pediatric patients

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