Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia.

Source:http://linkedlifedata.com/resource/pubmed/id/1463768

Biochim. Biophys. Acta 1992 Dec 10 1180 2 173-9

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PMID
1463768