Both paroxysmal nocturnal hemoglobinuria (PNH) type II cells and PNH type III cells can arise from different point mutations involving the same codon of the PIG-A gene [7]

Blood

Volumn 89, Issue 8, 1997, Pages 3069-3071

  Rollinson, S ^a   Richards, S ^a   Norfolk, D ^a   Bibi, K ^a   Morgan, G ^a   Hillmen, P ^a  

^a LEEDS GENERAL INFIRMARY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CYSTEINE; GENE PRODUCT;

AMINO ACID SUBSTITUTION; CASE REPORT; CODON; HUMAN; LETTER; PAROXYSMAL NOCTURNAL HEMOGLOBINURIA; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL;

EID: 0030935631     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v89.8.3069     Document Type: Letter

References (10)