Na Shen, Ting Wang, Delei Li, Aiguo Liu, & Yanjun Lu. (2019). Whole-exome sequencing identifies a novel missense variant within LOXHD1 causing rare hearing loss in a Chinese family. BMC.
Chicago Style (17th ed.) CitationNa Shen, Ting Wang, Delei Li, Aiguo Liu, and Yanjun Lu. Whole-exome Sequencing Identifies a Novel Missense Variant Within LOXHD1 Causing Rare Hearing Loss in a Chinese Family. BMC, 2019.
MLA (9th ed.) CitationNa Shen, et al. Whole-exome Sequencing Identifies a Novel Missense Variant Within LOXHD1 Causing Rare Hearing Loss in a Chinese Family. BMC, 2019.
Warning: These citations may not always be 100% accurate.