α‑thalassemia deletion [‑SEA(Southeast Asian)] and a compound heterozygote for the ChineseGγ+(Aγδβ)0/βCD17‑thalassemia mutation: A case report-Reference-Cited by-同舟云学术

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α‑thalassemia deletion [‑^SEA(Southeast Asian)] and a compound heterozygote for the Chinese^Gγ⁺(^Aγδβ)⁰/β^CD17‑thalassemia mutation: A case report

Published:2023-04-18 Issue:6 Volume:27 Page:
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:
Short-container-title:Mol Med Rep

Author:

Qian Hou¹,Li Weifeng¹,Lin Xiuhua¹,Xu Ji¹,Zhang Xiaoli¹,Zhao Weihua²,Wu Yike¹,Liu Wenlan¹

Affiliation:

1. The Center for Medical Genetics and Molecular Diagnosis, Shenzhen Second People's Hospital/The First Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen, Guangdong 518035, P.R. China

2. Prenatal Diagnosis Center, Shenzhen Second People's Hospital/The First Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen, Guangdong 518035, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Reference23 articles.

1. Thalassemias;Martin;Pediatr Clin North Am,2013

2. Molecular characterization of α- and β-thalassemia in the Yulin region of Southern China;He;Gene,2018

3. Beta-thalassemia;Cao;Genet Med,2010

4. Amelioration of Sardinian beta0 thalassemia by genetic modifiers;Galanello;Blood,2009

5. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand;Panyasai;Haematologica,2004

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