Wyniki wyszukiwania dla: Emmanuel Kanavakis
artykuł
Clinica Chimica Acta > 2015 > 446 > C > 241-247
Alpha-thalassaemia is an autosomal recessive disorder characterized by defective production of the alpha chain of haemoglobin. It is caused mainly by deletions of one or both of the duplicated alpha-globin genes on chromosome 16, and/or by nucleotide variations, known as “nondeletion” mutations. Definition of the alpha globin genotype in carriers supports genetic counselling, and in patients with...
