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

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Bibliographic Details
Published in:Blood 1997-04, Vol.89 (8), p.3069-2861
Main Authors: Rollinson, S, Richards, S, Norfolk, D, Bibi, K, Morgan, G, Hillmen, P
Format: Article
Language:English
Subjects:
Adult
Codon - genetics
Genetic Heterogeneity
Hemoglobinuria, Paroxysmal - genetics
Hemoglobinuria, Paroxysmal - pathology
Humans
Male
Membrane Proteins - deficiency
Membrane Proteins - genetics
Point Mutation
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ISSN:0006-4971
1528-0020
DOI:10.1182/blood.v89.8.3069