Severe erythrocyte adenylate kinase deficiency due to homozygous A -> G substitution at codon 164 of human AK1 gene associated with chronic haemolytic anaemia

Academic Article
Publication Date:
1997
Iris type:
01.01 Articolo in rivista
List of contributors:
Authors of the University:
Handle:
https://iris.cnr.it/handle/20.500.14243/236517
Published in:
BRITISH JOURNAL OF HAEMATOLOGY (PRINT)
Journal