β-spectrin promissao: A translation initiation codon mutation of the β-spectrin gene (ATG → GTG) associated with hereditary spherocytosis and spectrin deficiency in a Brazilian family [8]

Blood

Volumn 91, Issue 1, 1998, Pages 368-369

  Basseres, D S ^a   Vicentim, D L ^a   Costa, F F ^a   Saad, S T O ^a   Hassoun, H ^a  

^a UNIVERSITY OF CAMPINAS   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN; MEMBRANE PROTEIN; NUCLEOTIDE; SPECTRIN;

BLOOD SMEAR; CLINICAL ARTICLE; CODON; CONTROLLED STUDY; FAMILY STUDY; FEMALE; GENE; HEREDITARY SPHEROCYTOSIS; HUMAN; LETTER; MALE; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; PROTEIN DEFICIENCY; TRANSLATION INITIATION; ADULT; BRAZIL; CASE REPORT; DOMINANT GENE; GENETICS; NUCLEOTIDE SEQUENCE; PEDIGREE; POINT MUTATION; RNA TRANSLATION;

ADULT; BRAZIL; CODON; DNA MUTATIONAL ANALYSIS; FEMALE; GENES, DOMINANT; HUMANS; MALE; PEDIGREE; PEPTIDE CHAIN INITIATION, TRANSLATIONAL; POINT MUTATION; SPECTRIN; SPHEROCYTOSIS, HEREDITARY;

EID: 0031594649     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v91.1.368     Document Type: Letter

References (7)