Wang, J., Zhang, Q., Chen, Y., Yu, S., Wu, X., Bao, X., & Wen, Y. (2018). Novel MEF2C point mutations in Chinese patients with Rett (−like) syndrome or non-syndromic intellectual disability: Insights into genotype-phenotype correlation. BMC Med Genet.
শিকাগো স্টাইলে সাইটেশনWang, Jiaping, Qingping Zhang, Yan Chen, Shujie Yu, Xiru Wu, Xinhua Bao, এবং Yongxin Wen. "Novel MEF2C Point Mutations in Chinese Patients With Rett (−like) Syndrome or Non-syndromic Intellectual Disability: Insights Into Genotype-phenotype Correlation." BMC Med Genet 2018.
এমএলএ সাইটেশনWang, Jiaping, et al. "Novel MEF2C Point Mutations in Chinese Patients With Rett (−like) Syndrome or Non-syndromic Intellectual Disability: Insights Into Genotype-phenotype Correlation." BMC Med Genet 2018.