SILENT BETA-THALASSEMIA ASSOCIATED WITH HB KNOSSOS BETA-27 (B9) ALA-]SER IN ALGERIA

被引：9

作者：

ROUABHI, F

CHARDIN, P

BOISSEL, JP

BEGHOUL, F

LABIE, D

BENABADJI, M

机构：

[1] CHU COCHIN,INSERM,U15,INST PATHOL & BIOL CELLULAIRES & MOLEC,F-75674 PARIS 14,FRANCE

[2] CHU MUSTAPHA,CMI,ALGER,ALGERIA

来源：

HEMOGLOBIN | 1983年 / 7卷 / 06期

关键词：

D O I：

10.3109/03630268309027935

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：

引用

页码：555 / 561

页数：7

共 8 条

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BRITISH JOURNAL OF HAEMATOLOGY, 1980, 44 (04) :527-534

[2] STRUCTURAL STUDY OF HEMOGLOBIN KNOSSOS, BETA-27 (B9) ALA-]SER - A NEW ABNORMAL HEMOGLOBIN PRESENT AS A SILENT BETA-THALASSEMIA [J].

AROUS, N ;

GALACTEROS, F ;

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[3] SILENT BETA-THALASSEMIA CAUSED BY A SILENT BETA-CHAIN MUTANT - THE PATHOGENESIS OF A SYNDROME OF THALASSEMIA INTERMEDIA [J].

FESSAS, P ;

LOUKOPOULOS, D ;

LOUTRADIANAGNOSTOU, A ;

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BRITISH JOURNAL OF HAEMATOLOGY, 1982, 51 (04) :577-583

[4] SILENT NUCLEOTIDE SUBSTITUTION IN A BETA+-THALASSEMIA GLOBIN GENE ACTIVATES SPLICE SITE IN CODING SEQUENCE RNA [J].

GOLDSMITH, ME ;

HUMPHRIES, RK ;

LEY, T ;

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NIENHUIS, AW .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (08) :2318-2322

[5] A CATALOG OF SPLICE JUNCTION SEQUENCES [J].

MOUNT, SM .

NUCLEIC ACIDS RESEARCH, 1982, 10 (02) :459-472

[6] ABNORMAL RNA PROCESSING DUE TO THE EXON MUTATION OF BETA-E-GLOBIN GENE [J].

ORKIN, SH ;

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GOFF, SC ;

SEXTON, JP .

NATURE, 1982, 300 (5894) :768-769

[7]

TREISMAN R, 1983, NATURE, V302, P591, DOI 10.1038/302591a0

[8]

Weatherall D. J., 1981, THALASSEMIA SYNDROME

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