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American Journal of Human Genetics|January 25, 2011
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42Guntram Borck, Atteeq Ur Rehman, Kwanghyuk Lee, et al.Nature Genetics|August 31, 2010
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1Verneri Anttila, Hreinn Stefansson, Mikko Kallela, et al.Pageof 3