Publications
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[ Author] Title Year Filters: Author is Rehman, Atteeq U and Keyword is Phenotype [Clear All Filters]
Challenges and solutions for gene identification in the presence of familial locus heterogeneity. Eur J Hum Genet 23, 1207-15 (2015).
Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86. Am J Hum Genet 94, 144-52 (2014).