Twenty seven nucleotide deletion within exon 11 of the erythrocyte band 3 gene in Indonesian ovalocytosis

The Japanese Journal of Human Genetics

Volumn 39, Issue 1, 1994, Pages 181-185

  Takeshima, Yasuhiro ^a   Sofro, Abdul Salam ^b   Suryantoro, Purnomo ^b   Narita, Naoko ^a   Matsuo, Masafumi ^a  

^a KOBE UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b GADJAH MADA UNIVERSITY   (Indonesia)

Author keywords

band 3; erythrocyte; Indonesia; ovalocytosis

Indexed keywords

NUCLEOTIDE;

ARTICLE; CASE REPORT; ELLIPTOCYTOSIS; EXON; GENE AMPLIFICATION; GENE DELETION; HUMAN; NUCLEOTIDE SEQUENCE;

ANION EXCHANGE PROTEIN 1, ERYTHROCYTE; BASE SEQUENCE; ELLIPTOCYTOSIS, HEREDITARY; ERYTHROCYTE MEMBRANE; EXONS; HUMAN; INDONESIA; MOLECULAR SEQUENCE DATA; OLIGONUCLEOTIDES; POLYMERASE CHAIN REACTION; SEQUENCE DELETION; SUPPORT, NON-U.S. GOV'T;

EID: 0028181373     PISSN: 09168478     EISSN: 1435232X     Source Type: Journal    
DOI: 10.1007/BF01915953     Document Type: Article

References (11)

1. Why are some genetic diseases common?
2. Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosis
3. Band 3 Memphis: A widespread polymorphism with abnormal electrophoretic mobility of erythrocyte band 3 protein caused by AAG→GAG (Lys→Glu) in codon 56
4. Exon skipping during splicing of dystrophin mRNA precursor due to an intraexon deletion in the dystrophin gene of Duchenne muscular dystrophy Kobe
5. Molecular basis for membrane rigidity of hereditary ovalocytosis: A novel mechanism involving the cytoplasmic domain of band 3
6. Defective anion transport activity of the abnormal band 3 in hereditary ovalocytic red blood cells
7. Basis of unique red cell membrane properties in hereditary ovalocytosis
8. Ovalocytosis in Indonesia
9. A postulated mechanism for deletions with inversions
10. Melanesian hereditary ovalocytes have a deletion in red cell band 3
11. The complete amino acid sequence of the human erythrocyte membrane amino-transport protein deduced from the cDNA sequence