Connexin-26 mutations in sporadic and inherited sensorineural deafness. - Estvill,X.; Fortina,P.; Surrey,S.; Rabionet,R.; Melchionda,S.; D’Agruma,L.; Mansfield,F.; Rappaport,E.; Govea,N.; Milà,M.; Zelante,L.; Gasparini,P. (Lancet, 1998)