HB AL-AIN ABU-DHABI [ALPHA-18(A16)GLY-]ASP] - A NEW HEMOGLOBIN-VARIANT DISCOVERED IN AN EMIRATEE FAMILY

被引:9
作者
ABBES, S
MRAD, A
FITZGERALD, PA
DORMER, P
BLOUQUIT, Y
KISTER, J
GALACTEROS, F
WAJCMAN, H
机构
[1] HOP BICETRE,INSERM,U299,F-94275 LE KREMLIN BICETR,FRANCE
[2] AL TAWAM HOSP,DEPT HEMATOL,AL AIN,U ARAB EMIRATES
[3] HOP HENRI MONDOR,INSERM,U91,F-94010 CRETEIL,FRANCE
[4] AL TAWAM HOSP,DEPT INTERNAL MED,AL AIN,U ARAB EMIRATES
关键词
D O I
10.3109/03630269209005687
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During a routine program of hemoglobin screening performed in the United Arab Emirates, we observed an electrophoretically fast-moving variant in a 9-month-old girl and in several members of her family. The structural determination, performed by reversed phase high performance liquid chromatography and amino acid sequencing, revealed a new variant that we named Hb Al-Ain Abu Dhabi [alpha-18(A16) Gly-->Asp]. Its functional properties were normal.
引用
收藏
页码:355 / 362
页数:8
相关论文
共 14 条
  • [11] RADOLA BJ, 1973, ANN NY ACAD SCI, V209, P127, DOI 10.1111/j.1749-6632.1973.tb47523.x
  • [12] SCHNEIDER RG, 1986, CRC HDB SERIES, V4, P125
  • [13] CLEAVAGE BY PROTEASE FROM STAPHYLOCOCCUS-AUREUS V8 - AN IMPROVEMENT IN THE SEQUENCE-ANALYSIS OF HUMAN HEMOGLOBIN-VARIANTS
    VASSEUR, C
    GALACTEROS, F
    GROFF, P
    WAJCMAN, H
    [J]. JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 1991, 22 (03): : 195 - 205
  • [14] RED-CELL GENETIC ABNORMALITIES IN PENINSULAR ARABS - SICKLE HEMOGLOBIN, G6PD DEFICIENCY, AND ALPHA-THALASSEMIA AND BETA-THALASSEMIA
    WHITE, JM
    BYRNE, M
    RICHARDS, R
    BUCHANAN, T
    KATSOULIS, E
    WEERASINGH, K
    [J]. JOURNAL OF MEDICAL GENETICS, 1986, 23 (03) : 245 - 251