β-thalassemia intermedia resulting from compound heterozygosity for an IVSI-1 (G-A) and a silent 5'UTR +33 (C-G) mutation

Haematologica

Volumn 85, Issue 4, 2000, Pages 443-441

  Bento, M C ^a   Ribeiro, M L ^a   Cunha, E ^a   Goncalves, P ^a   Martin Nunez, G ^a   Tamagnini, G ^a  

^a CENTRO HOSPITALAR E UNIVERSITÁRIO DE COIMBRA   (Portugal)

Author keywords

Silent thalassemia; Thalassemia intermedia

Indexed keywords

BETA GLOBIN;

5' UNTRANSLATED REGION; ARTICLE; BETA THALASSEMIA; CASE REPORT; CAUCASIAN; DNA SEQUENCE; FAMILY HISTORY; FEMALE; GENE MUTATION; GLOBIN GENE; HAPLOTYPE; HEMATOLOGICAL PARAMETERS; HETEROZYGOSITY; HUMAN; FAMILY HEALTH; GENETICS; HETEROZYGOTE DETECTION; LETTER; MIDDLE AGED; NUCLEOTIDE SEQUENCE; PHENOTYPE; POINT MUTATION; SPAIN; SPLENECTOMY;

BETA-THALASSEMIA; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; HETEROZYGOTE DETECTION; HUMANS; MIDDLE AGED; PHENOTYPE; POINT MUTATION; SPAIN; SPLENECTOMY;

EID: 0034170499     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)