A Cao

Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin gene.

R. Casu, J. Lavinha, G. Loudianos, 1992, Blood.

Prenatal diagnosis of beta-thalassemia. Detection of a single nucleotide mutation in DNA.

Y W Kan, Y. Kan, M. Pirastu, 1983, The New England journal of medicine.

Molecular characterization of Wilson disease in the Sardinian population—Evidence of a founder effect

A. Angius, G. Loudianos, V. Dessì, 1999, Human mutation.