Retarded and aberrant splicings caused by single exon mutation in a phosphoglycerate kinase variant

Archives of Biochemistry and Biophysics

Volumn 327, Issue 1, 1996, Pages 35-40

  Ookawara, Tomomi ^a   Davé, Vibha ^a   Willems, Patrick ^b   Martin, Jean Jacques ^b   De Barsy, Thierry ^c   Matthys, Ervé ^d   Yoshida, Akira ^a  

^a CITY OF HOPE NATIONAL MEDICAL CENTER   (United States)

^b UNIVERSITY OF ANTWERP   (Belgium)

^c International Institute of Cellular and Molecular Pathology   (Belgium)

^d General Hospital St Jan   (Belgium)

Author keywords

enzyme deficiency; exon mutation; mRNA splicing; phosphoglycerate kinase variant

Indexed keywords

INITIATION FACTOR; PHOSPHOGLYCERATE KINASE;

ADOLESCENT; AMINO ACID ANALYSIS; AMINO ACID SUBSTITUTION; ARTICLE; CARBOXY TERMINAL SEQUENCE; CASE REPORT; CODON; ENZYME ACTIVITY; ENZYME DEFICIENCY; GENE DELETION; GENE MUTATION; HUMAN; HUMAN CELL; LYMPHOBLASTOID CELL; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RNA SPLICING;

EID: 0030020690     PISSN: 00039861     EISSN: None     Source Type: Journal    
DOI: 10.1006/abbi.1996.0089     Document Type: Article

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