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Wang SK, Hu Y, Yang J, et al. Fam83h null mice support a neomorphic mechanism for human ADHCAI. Mol Genet Genomic Med. 2015;4(1):46-67doi: 10.1002/mgg3.178.
Wang, S. K., Hu, Y., Yang, J., Smith, C. E., Richardson, A. S., Yamakoshi, Y., Lee, Y. L., Seymen, F., Koruyucu, M., Gencay, K., Lee, M., Choi, M., Kim, J. W., Hu, J. C., & Simmer, J. P. (2016). Fam83h null mice support a neomorphic mechanism for human ADHCAI. Molecular genetics & genomic medicine, 4(1), 46-67. https://doi.org/10.1002/mgg3.178
Wang, Shih-Kai, et al. "Fam83h null mice support a neomorphic mechanism for human ADHCAI." Molecular genetics & genomic medicine vol. 4,1 (2016): 46-67. doi: https://doi.org/10.1002/mgg3.178
Wang SK, Hu Y, Yang J, Smith CE, Richardson AS, Yamakoshi Y, Lee YL, Seymen F, Koruyucu M, Gencay K, Lee M, Choi M, Kim JW, Hu JC, Simmer JP. Fam83h null mice support a neomorphic mechanism for human ADHCAI. Mol Genet Genomic Med. 2015 Sep 21;4(1):46-67. doi: 10.1002/mgg3.178. eCollection 2016 Jan. PMID: 26788537; PMCID: PMC4707031.
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