A newly-characterized α-thalassaemia-1 deletion removes the entire α-like globin gene cluster in an Italian family
- Author
- FORTINA, P1 ; DIANZANI, I; SERRA, A; GOTTARDI, E; SAGLIO, G; FARINASSO, L; PIGA, A; GABUTTI, V; CAMASCHELLA, C
[1] Univ. degli studi, ist. clin. pediatrica, Torino 10126, Italy - Source
British journal of haematology. 1991, Vol 78, Num 4, pp 529-534 ; ref : 1/2 p
- CODEN
- BJHEAL
- ISSN
- 0007-1048
- Scientific domain
- Medical oncology; Hematology
- Publisher
- Blackwell, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Biologie moléculaire Chaîne peptidique α Délétion Exploration Globine Gène Homme Hémoglobinopathie Hémopathie Maladie héréditaire Mutation Thalassémie α
- Keyword (en)
- Molecular biology Alpha-Peptide chain Deletion Exploration Globin Gene Human Hemoglobinopathy Hemopathy Genetic disease Mutation α-Thalassemia
- Keyword (es)
- Biología molecular Cadena peptídica α Deleción Exploración Globina Gen Hombre Hemoglobinopatía Hemopatía Enfermedad hereditaria Mutación Talasemia α
- 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
- 4950681
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
10.1111/j.1365-2141.1991.tb04483.x 
https://dx.doi.org/10.1111/j.1365-2141.1991.tb04483.x
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