Shi, X., Zhang, Y., Qiu, S., Zhuang, W., Yuan, N., Sun, T., . . . Liu, K. (2018). A Novel GJB2 compound heterozygous mutation c.257C>G (p.T86R)/c.176del16 (p.G59A fs*18) causes sensorineural hearing loss in a Chinese family. J Clin Lab Anal.
Stile di citazione ChicagoShi, Xi, Yan Zhang, Shiwei Qiu, Wei Zhuang, Na Yuan, Tiantian Sun, Jian Gao, Yuehua Qiao, e Ke Liu. "A Novel GJB2 Compound Heterozygous Mutation C.257C>G (p.T86R)/c.176del16 (p.G59A Fs*18) Causes Sensorineural Hearing Loss in a Chinese Family." J Clin Lab Anal 2018.
Citazione MLAShi, Xi, et al. "A Novel GJB2 Compound Heterozygous Mutation C.257C>G (p.T86R)/c.176del16 (p.G59A Fs*18) Causes Sensorineural Hearing Loss in a Chinese Family." J Clin Lab Anal 2018.
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