A β-Thalassemia mutation found in Korea
- Author
- KOO, M. S; KIM, S. I; CHO, H. I; HATTORI, Y; YAMASHIRO, Y; HOSHITANI, M; OHBA, Y; MIYAJI, T; YAMAMOTO, KU; YAMAMOTO, KI
Kan-Nam gen. hosp., dep. clin. pathology, 135-090 Seoul, Korea, Republic of - Source
Hemoglobin. 1992, Vol 16, Num 4, pp 313-320 ; ref : 15 ref
- CODEN
- HEMOD8
- ISSN
- 0363-0269
- Scientific domain
- Genetics; Hematology
- Publisher
- Dekker, Monticello, NY
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Anémie hémolytique Chaîne peptidique β Codon Etude familiale Globine Gène Homme Mutation Thalassémie β Corée Hémoglobinopathie Hémopathie Maladie héréditaire Asie
- Keyword (en)
- Hemolytic anemia Beta-Peptide chain Codon Family study Globin Gene Human Mutation β-Thalassemia Korea Hemoglobinopathy Hemopathy Genetic disease Asia
- Keyword (es)
- Anemia hemolítica Cadena peptídica β Codón Estudio familiar Globina Gen Hombre Mutación Talasemia β Corea Hemoglobinopatía Hemopatía Enfermedad hereditaria Asia
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19A Diseases of red blood cells / 002B19A01 Anemias. Hemoglobinopathies
- Discipline
- Blood diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 5338043
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.3109/03630269208998875 
https://dx.doi.org/10.3109/03630269208998875
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