Hb Siriraj: A G→A substitution at codon 7 of the β-globin chain creates an MboII cutting site

Hemoglobin

Volumn 23, Issue 2, 1999, Pages 197-199

  Chang, Jan Gowth ^a   Yang, T Y ^a   Perng, L I ^a   Wang, N M ^a   Peng, C T ^a   Tsai, C H ^a  

^a CHINA MEDICAL UNIVERSITY HOSPITAL   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

BETA GLOBIN; HEMOGLOBIN VARIANT;

ARTICLE; CASE REPORT; ELECTROPHORESIS; GENE AMPLIFICATION; GENE MUTATION; HEMOGLOBIN DETERMINATION; HEMOGLOBINOPATHY; HETEROZYGOSITY; HUMAN; NUCLEIC ACID BASE SUBSTITUTION; TAIWAN;

EID: 0032915048     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.3109/03630269908996166     Document Type: Article

References (4)

1. Tuchinda, S., Beale, D., and Lehmann, H.: A new haemoglobin in a Thai family. A case of haemoglobin Siriraj-β-thalassaemia. Br. Med. J., 1:1583-1585, 1965.
2. Blackwell, R.Q., Liu, C.S., and Wang, C.L.: Haemoglobin Siriraj-β (A4) Glu→Lys in a Chinese subject in Taiwan. Vox Sang, 23:433-438, 1972.
3. Jen, P.C.: Abnormal hemoglobins found in Guangdong, P.R. China. Hemoglobin, 11:573-579, 1987.
4. Chiou, S.S., Chang, T.T., Chen, P.H., Lee, L.S., Chen, T.S., and Chang, J.G.: Molecular basis and haematological characterization of β thalassaemia major on Taiwan. Br. J. Haematol., 83:112, 1993.