Aminoglycoside-associated nonsyndromic deafness and speech disorder in mitochondrial A1555G mutation in a family: A case report.

MLA

Ou, Yang-Hao, et al. “Aminoglycoside-Associated Nonsyndromic Deafness and Speech Disorder in Mitochondrial A1555G Mutation in a Family: A Case Report.” Medicine, vol. 97, no. 42, Oct. 2018, p. e12878. EBSCOhost, https://doi.org/10.1097/MD.0000000000012878.

APA

Ou, Y.-H., Chen, A. W.-G., Fan, J.-Y., Cheng, W.-L., Lin, T.-T., Chen, M.-K., & Liu, C.-S. (2018). Aminoglycoside-associated nonsyndromic deafness and speech disorder in mitochondrial A1555G mutation in a family: A case report. Medicine, 97(42), e12878. https://doi.org/10.1097/MD.0000000000012878

Chicago

Ou, Yang-Hao, Andy Wei-Ge Chen, Jun-Yang Fan, Wen-Ling Cheng, Ta-Tsung Lin, Mu-Kuan Chen, and Chin-San Liu. 2018. “Aminoglycoside-Associated Nonsyndromic Deafness and Speech Disorder in Mitochondrial A1555G Mutation in a Family: A Case Report.” Medicine 97 (42): e12878. doi:10.1097/MD.0000000000012878.