Hereditary spherocytosis due to band 3 deficiency: 15 novel mutations in SLC4A1

American Journal of Hematology

Volumn 88, Issue 2, 2013, Pages 159-160

  Van Zwieten, Rob ^a   François, Jerney J J M ^b   Van Leeuwen, Karin ^a   Van Wesel, Annet C W ^b   Van Bruggen, Robin ^a   Van Solinge, Wouter W ^b   Roos, Dirk ^a   Verhoeven, Arthur J ^c   Van Wijk, Richard ^b  

^a CENTRAL LABORATORY   (Netherlands)

^b UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^c UNIVERSITY OF AMSTERDAM   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; EOSINO 5' MALEIMIDE; ERYTHROCYTE BAND 3 PROTEIN; GLYCINE; MALEIMIDE DERIVATIVE; MEMBRANE PROTEIN; SLC4A1 PROTEIN; SPECTRIN; THREONINE; UNCLASSIFIED DRUG;

ALLELE; AUTOSOMAL DOMINANT DISORDER; DNA SEQUENCE; ERYTHROCYTE; ERYTHROCYTE DISORDER; EXON; GENE EXPRESSION; GENE MUTATION; GENETIC ANALYSIS; HEREDITARY HEMOLYTIC ANEMIA; HEREDITARY SPHEROCYTOSIS; HISTOPATHOLOGY; HUMAN; INTRON; LETTER; PATIENT SELECTION; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; PROTEIN BINDING;

ALLELES; ANION EXCHANGE PROTEIN 1, ERYTHROCYTE; COHORT STUDIES; DNA MUTATIONAL ANALYSIS; EXONS; GENETIC ASSOCIATION STUDIES; HETEROZYGOTE; HUMANS; INTRONS; MUTATION; RNA, MESSENGER; SPECTRIN; SPHEROCYTOSIS, HEREDITARY;

EID: 84872909554     PISSN: 03618609     EISSN: 10968652     Source Type: Journal    
DOI: 10.1002/ajh.23363     Document Type: Letter

References (0)