Thalassemia intermedia due to a novel mutation in the second intervening sequence of the β-globin gene

Hemoglobin

Volumn 31, Issue 4, 2007, Pages 433-438

  Agouti, Imane ^a   Bennani, Mohcine ^a   Ahmed, Abouyoub ^b   Barakat, Amina ^a   Mohamed, Khattab ^c   Badens, Catherine ^d,e  

^a ABDELMALEK ESSAADI UNIVERSITY   (Morocco)

^b IBN SINA HOSPITAL   (Morocco)

^c Hopital d'Enfants   (Morocco)

^d TIMONE HOSPITAL   (France)

^e AIX MARSEILLE UNIVERSITY   (France)

Author keywords

Thalassemia (thal) intermedia; Mutations; Second intervening sequence (IVS II)

Indexed keywords

BETA GLOBIN;

3' UNTRANSLATED REGION; ARTICLE; BETA THALASSEMIA; CASE REPORT; DISEASE ASSOCIATION; GENE LOCATION; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; HAPLOTYPE; HOMOZYGOSITY; HUMAN; MALE; MOROCCO; PATHOPHYSIOLOGY; PHENOTYPE; SCHOOL CHILD;

ADULT; BETA-THALASSEMIA; CHILD; FEMALE; GLOBINS; HAPLOTYPES; HOMOZYGOTE; HUMANS; INTRONS; MALE; MUTATION;

EID: 36248933650     PISSN: 03630269     EISSN: 1532432X     Source Type: Journal    
DOI: 10.1080/03630260701613210     Document Type: Article

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