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    Luping Zhang, Lingxiang Hu, Yongchuan Chai, Xiuhong Pang, Tao Yang, Hao Wu, A Dominant Mutation in the Stereocilia-Expressing Gene TBC1D24 is a Probable Cause for Nonsyndromic Hearing Impairment, Human Mutation, 2014, 35, 7
  2. 2
    Hamid Saeed, Haplotype analysis of DFNB8/10 locus reveals contribution of TMPRSS3 mutations in Pakistani deaf population, Genes & Genomics, 2014, 36, 2, 143

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    Atteeq U. Rehman, Regie Lyn P. Santos-Cortez, Robert J. Morell, Meghan C. Drummond, Taku Ito, Kwanghyuk Lee, Asma A. Khan, Muhammad Asim R. Basra, Naveed Wasif, Muhammad Ayub, Rana A. Ali, Syed I. Raza, Deborah A. Nickerson, Jay Shendure, Michael Bamshad, Saima Riazuddin, Neil Billington, Shaheen N. Khan, Penelope L. Friedman, Andrew J. Griffith, Wasim Ahmad, Sheikh Riazuddin, Suzanne M. Leal, Thomas B. Friedman, Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86, The American Journal of Human Genetics, 2014, 94, 1, 144

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