APA

Liu S., Xie L., Yue J., Ma T., Peng C., Qiu B., Yang Z. & Yang J. (20170228). Whole-exome sequencing identifies a novel homozygous frameshift mutation in the PROM1 gene as a causative mutation in two patients with sporadic retinitis pigmentosa. : International journal of molecular medicine.

Chicago

Liu Sanmei, Xie Lan, Yue Jun, Ma Tao, Peng Chunyan, Qiu Biyuan, Yang Zhenglin and Yang Jiyun. 20170228. Whole-exome sequencing identifies a novel homozygous frameshift mutation in the PROM1 gene as a causative mutation in two patients with sporadic retinitis pigmentosa. : International journal of molecular medicine.

Harvard

Liu S., Xie L., Yue J., Ma T., Peng C., Qiu B., Yang Z. and Yang J. (20170228). Whole-exome sequencing identifies a novel homozygous frameshift mutation in the PROM1 gene as a causative mutation in two patients with sporadic retinitis pigmentosa. : International journal of molecular medicine.

MLA

Liu Sanmei, Xie Lan, Yue Jun, Ma Tao, Peng Chunyan, Qiu Biyuan, Yang Zhenglin and Yang Jiyun. Whole-exome sequencing identifies a novel homozygous frameshift mutation in the PROM1 gene as a causative mutation in two patients with sporadic retinitis pigmentosa. : International journal of molecular medicine. 20170228.