Xia, H., Huang, X., Xu, H., Zhou, Y., Gong, L., Yang, Z., . . . Deng, H. (2019). GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorder. Genet Mol Biol.
Stile di citazione ChicagoXia, Hong, Xiangjun Huang, Hongbo Xu, Yong-an Zhou, Lina Gong, Zhijian Yang, Jingyan Lv, e Hao Deng. "GJB2 C.235delC Variant Associated With Autosomal recessive Nonsyndromic Hearing Loss and Auditory Neuropathy Spectrum disorder." Genet Mol Biol 2019.
Citazione MLAXia, Hong, et al. "GJB2 C.235delC Variant Associated With Autosomal recessive Nonsyndromic Hearing Loss and Auditory Neuropathy Spectrum disorder." Genet Mol Biol 2019.
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