Targeted exome sequencing reveals novel USH2A mutations in Chinese patients with simplex Usher syndrome.

MLA

Hai-Rong Shu, et al. “Targeted Exome Sequencing Reveals Novel USH2A Mutations in Chinese Patients with Simplex Usher Syndrome.” BMC Medical Genetics, vol. 16, no. 1, Sept. 2015, pp. 1–5. EBSCOhost, https://doi.org/10.1186/s12881-015-0223-9.

APA

Hai-Rong Shu, Huai Bi, Yang-Chun Pan, Hang-Yu Xu, Jian-Xin Song, & Jie Hu. (2015). Targeted exome sequencing reveals novel USH2A mutations in Chinese patients with simplex Usher syndrome. BMC Medical Genetics, 16(1), 1–5. https://doi.org/10.1186/s12881-015-0223-9

Chicago

Hai-Rong Shu, Huai Bi, Yang-Chun Pan, Hang-Yu Xu, Jian-Xin Song, and Jie Hu. 2015. “Targeted Exome Sequencing Reveals Novel USH2A Mutations in Chinese Patients with Simplex Usher Syndrome.” BMC Medical Genetics 16 (1): 1–5. doi:10.1186/s12881-015-0223-9.