Werner syndrome: identification of the homozygous g.nt 77177 a>g mutation(Genbank acc# AY44237) in the WRN gene in two apparently unrelated italian families from Sardinia suggests a founder effect / Masala, M., Olivieri, C., Pirodda, C., Cottoni, F.M.G., Danesino, C., Cerimele, D., Scappaticci, S.. - (2005).
Werner syndrome: identification of the homozygous g.nt 77177 a>g mutation(Genbank acc# AY44237) in the WRN gene in two apparently unrelated italian families from Sardinia suggests a founder effect
COTTONI, Francesca Maria Giovanna;
2005-01-01
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