The Ivs-1-110 (G→T) and Codon 39 (C→T) β-Thalassemia Mutations in Association with α-Thal-2 (−3.7 Kb) and Hb Hasharon [α47(CE5)Asp→His] in a Brazilian Patient

Autor:	C. S. B. Martins, Fernando Ferreira Costa, M. S. Figueredo, E. M. Kimura, Maria de Fátima Sonati
Rok vydání:	1992
Předmět:	Hemolytic anemia Genetics Hb Hasharon Thalassemia Biochemistry (medical) Clinical Biochemistry Intron Hematology Biology medicine.disease Hemoglobinopathy Mutation (genetic algorithm) medicine Globin Genetics (clinical)
Zdroj:	Hemoglobin. 16:525-528
ISSN:	1532-432X 0363-0269
DOI:	10.3109/03630269208993122
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::9f5e1be7744da29ae2690ba89d3495f0 https://doi.org/10.3109/03630269208993122 Zobrazit plný text záznamu