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A Novel Mutation at HBB: c.91delA (Codon 30, -A) Causing ß-Thalassemia in a Chinese Family.
Jia, Wenguang; Wang, Weidong; Zhu, Hengying; Chen, Ping.
Affiliation
  • Jia W; Department of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Guangxi Key Laboratory of Thalassemia Research, Nanning, China.
  • Wang W; Guangxi Medical University, Nanning, China.
  • Zhu H; The First Affiliated Hospital of Guangxi Medical University, Guangxi Key Laboratory of Thalassemia Research, Nanning, China.
  • Chen P; The First Affiliated Hospital of Guangxi Medical University, Guangxi Key Laboratory of Thalassemia Research, Nanning, China, chenping@gxmu.edu.cn.
Acta Haematol ; 142(4): 249-252, 2019.
Article in En | MEDLINE | ID: mdl-31108495
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Codon / Hemoglobins / Base Sequence / Family / Sequence Deletion / Beta-Thalassemia Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Acta Haematol Year: 2019 Document type: Article Affiliation country: China Country of publication: Suiza
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Codon / Hemoglobins / Base Sequence / Family / Sequence Deletion / Beta-Thalassemia Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Acta Haematol Year: 2019 Document type: Article Affiliation country: China Country of publication: Suiza