Coinheritance of α- and β-spectrin gene mutations in a case of hereditary elliptocytosis [3]

Blood

Volumn 92, Issue 11, 1998, Pages 4481-4482

  Dhermy, D ^a   Galand, C ^a   Bournier, O ^a   King, M J ^a   Cynober, T ^a   Roberts, I ^a   Kanyike, F ^a   Adekile, A ^a  

^a INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

FODRIN; SPECTRIN;

CASE REPORT; ELLIPTOCYTOSIS; ERYTHROCYTE MEMBRANE; FAMILY STUDY; GENE MUTATION; GENETIC DISORDER; HEREDITARY ELLIPTOCYTOSIS; HUMAN; HUMAN CELL; LETTER; PRIORITY JOURNAL; RETICULOCYTE COUNT;

EID: 0032400880     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v92.11.4481     Document Type: Letter

References (11)