Manolis E N, Yandavi N, Nadol J B, Eavey R D, McKenna M, Rosenbaum S, Khetarpal U, Halpin C, Merchant S N, Duyk G M, MacRae C, Seidman C E, Seidman J G
Department of Otolaryngology, Massachusetts Eye and Ear Infirmary, Boston, MA, USA.
Hum Mol Genet. 1996 Jul;5(7):1047-50. doi: 10.1093/hmg/5.7.1047.
We report a novel locus responsible for postlingual progressive sensorineural hearing loss (designated DFNA9) that maps to chromosome 14q12-13. A large kindred with autosomal dominant transmission of non-syndromic hearing loss was clinically studied. Hearing in affected individuals deteriorated at approximately 20 years of age and progressed to anacusis in the fifth decade. A random genome-wide search using polymorphic short tandem repeats demonstrated linkage with D14S121 (maximum two point LOD score = 6.19, theta = 0). Haplotype analysis of recombination events defined a 9 cM disease interval, between D14S252 and D14S49.
我们报告了一个导致语后进行性感音神经性听力损失(命名为DFNA9)的新基因座,它定位于染色体14q12 - 13。对一个具有常染色体显性遗传非综合征性听力损失的大家族进行了临床研究。受影响个体的听力在约20岁时开始恶化,并在第五个十年发展为全聋。使用多态性短串联重复序列进行全基因组随机搜索,结果显示与D14S121连锁(最大两点LOD分数 = 6.19,θ = 0)。对重组事件的单倍型分析确定了一个9厘摩的疾病区间,位于D14S252和D14S49之间。