Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleNovel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families.AuthorsYuan, H. J.; Han, D. Y.; Sun, Q.; Yan, D.; Sun, H. J.; Tao, R.; Cheng, J.; Qin, W.; Angeli, S.; Ouyang, X. M.; Yang, S. Z.; Feng, L.; Cao, J. Y.; Feng, G. Y.; Wang, Y. F.; Dai, P.; Zhai, S. Q; Yang, W. Y.; He, L.; Liu, X. Z.AbstractA letter to the editor on a study that reveals higher percentage of Chinese family with late-onset autosomal dominant non-syndromic progressive sensorineural hearing loss is presented.SubjectsLETTERS to the editor; SENSORINEURAL hearing lossPublicationClinical Genetics, 2008, Vol 73, Issue 4, p391ISSN0009-9163Publication typeLetterDOI10.1111/j.1399-0004.2008.00972.x