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Journal of Medical Genetics|August 6, 2002
A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qterS H Blanton, C Y Liang, M W Cai, et al.Clinical Genetics|September 18, 2007
A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese familyJ Cheng, D Y Han, P Dai, et al.Pageof 3