Homozygous mutation in PTRH2 gene causes progressive sensorineural deafness and peripheral neuropathy.

MLA

Sharkia, Rajech, et al. “Homozygous Mutation in PTRH2 Gene Causes Progressive Sensorineural Deafness and Peripheral Neuropathy.” American Journal of Medical Genetics. Part A, vol. 173, no. 4, Apr. 2017, pp. 1051–55. EBSCOhost, https://doi.org/10.1002/ajmg.a.38140.

APA

Sharkia, R., Shalev, S. A., Zalan, A., Marom, D. M., Watemberg, N., Urquhart, J. E., Daly, S. B., Bhaskar, S. S., Williams, S. G., Newman, W. G., Spiegel, R., Azem, A., Elpeleg, O., & Mahajnah, M. (2017). Homozygous mutation in PTRH2 gene causes progressive sensorineural deafness and peripheral neuropathy. American Journal of Medical Genetics. Part A, 173(4), 1051–1055. https://doi.org/10.1002/ajmg.a.38140

Chicago

Sharkia, Rajech, Stavit A. Shalev, Abdelnaser Zalan, David, Milit Marom, Nathan Watemberg, Jill E. Urquhart, Sarah B. Daly, et al. 2017. “Homozygous Mutation in PTRH2 Gene Causes Progressive Sensorineural Deafness and Peripheral Neuropathy.” American Journal of Medical Genetics. Part A 173 (4): 1051–55. doi:10.1002/ajmg.a.38140.