Rare β-thalassemia mutations in Asian Indians

American Journal of Hematology

Volumn 65, Issue 4, 2000, Pages 322-323

  Agarwal, Sarita ^a   Hattori, Y ^b   Agarwal, S S ^a  

^a SANJAY GANDHI POSTGRADUATE INSTITUTE OF MEDICAL SCIENCES   (India)

^b YAMAGUCHI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

thalassemia; Asian Indians; Prenatal diagnosis

Indexed keywords

ARTICLE; ASIAN; BETA THALASSEMIA; CLINICAL ARTICLE; DISEASE ASSOCIATION; GENE MUTATION; HETEROZYGOTE; HUMAN; INDIAN; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ASIA; BETA-THALASSEMIA; HUMANS; MUTATION;

EID: 0033730254     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8652(200012)65:4<322::AID-AJH14>3.0.CO;2-2     Document Type: Article

References (8)

1. Codon 4 T-A, Codon 5 C-T and Codon 6 G-T mutations in cis position: A form of thalassemia trait
2. A novel Indian β-thalassemia mutation: Hb Lucknow [β8 (A5) Lys-Arg]
3. Identification of new frameshift mutation in an Asian Indian
4. Geo-ethinic distribution of beta thalassemia mutations in Uttar Pradesh, India
5. Rare β-thalassemia mutations in Asian Indians
6. Frameshift codon 5 (-CT) thalassemia: A novel mutation detected in a Greek patient
7. The molecular basis of β-thalassemia in Bulgaria
8. The molecular basis of β-thalassemia in Punjab and Maharashtrian Indians includes a multilocus etiology involving triplicate α-globin loci