Styl cytowania APA

Lin, Y., Lin, Y., Lu, Y., Liu, T., Chen, C., Hsu, C., . . . Wu, C. (2017). A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss. Sci Rep.

Styl cytowania Chicago

Lin, Yin-Hung, Yi-Hsin Lin, Ying-Chang Lu, Tien-Chen Liu, Chien-Yu Chen, Chuan-Jen Hsu, Pei-Lung Chen, i Chen-Chi Wu. "A Novel Missense Variant in the Nuclear Localization Signal of POU4F3 Causes Autosomal Dominant Non-syndromic Hearing Loss." Sci Rep 2017.

Styl cytowania MLA

Lin, Yin-Hung, et al. "A Novel Missense Variant in the Nuclear Localization Signal of POU4F3 Causes Autosomal Dominant Non-syndromic Hearing Loss." Sci Rep 2017.

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