Connexin-26 mutations in sporadic and inherited sensorineural deafness.
Estivill, Xavier; Fortina, Paolo; Surrey, Saul; Rabionet, Raquel; Melchionda, Salvatore; D'Agruma, Leonardo; Mansfield, Elaine; Rappaport, Eric; Govea, Nancy; Mila, Montse; Zelante, Leopoldo; Gasparini, Paolo; Estivill, X; Fortina, P; Surrey, S; Rabionet, R; Melchionda, S; D'Agruma, L; Mansfield, E; Rappaport, E; Lancet, 1998, vol. 351, issue 9100, p 394, ISSN 00995355. ISBN 00995355.

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