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Poulter JA, Ali M, Gilmour DF, et al. Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy. Am J Hum Genet. 2016;98(3):592doi: 10.1016/j.ajhg.2016.02.017.
Poulter, J. A., Ali, M., Gilmour, D. F., Rice, A., Kondo, H., Hayashi, K., Mackey, D. A., Kearns, L. S., Ruddle, J. B., Craig, J. E., Pierce, E. A., Downey, L. M., Mohamed, M. D., Markham, A. F., Inglehearn, C. F., & Toomes, C. (2016). Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy. American journal of human genetics, 98(3), 592. https://doi.org/10.1016/j.ajhg.2016.02.017
Poulter, James A, et al. "Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy." American journal of human genetics vol. 98,3 (2016): 592. doi: https://doi.org/10.1016/j.ajhg.2016.02.017
Poulter JA, Ali M, Gilmour DF, Rice A, Kondo H, Hayashi K, Mackey DA, Kearns LS, Ruddle JB, Craig JE, Pierce EA, Downey LM, Mohamed MD, Markham AF, Inglehearn CF, Toomes C. Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy. Am J Hum Genet. 2016 Mar 03;98(3):592. doi: 10.1016/j.ajhg.2016.02.017. Epub 2016 Mar 03. PMID: 28863275; PMCID: PMC4800049.
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