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Watson LM, Bamber E, Schnekenberg RP, et al. Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44. Am J Hum Genet. 2017;101(4):638doi: 10.1016/j.ajhg.2017.09.006.
Watson, L. M., Bamber, E., Schnekenberg, R. P., Williams, J., Bettencourt, C., Jayawant, S., Lickiss, J., Fawcett, K., Clokie, S., Wallis, Y., Clouston, P., Sims, D., Houlden, H., Becker, E. B. E., & Németh, A. H. (2017). Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44. American journal of human genetics, 101(4), 638. https://doi.org/10.1016/j.ajhg.2017.09.006
Watson, Lauren M, et al. "Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44." American journal of human genetics vol. 101,4 (2017): 638. doi: https://doi.org/10.1016/j.ajhg.2017.09.006
Watson LM, Bamber E, Schnekenberg RP, Williams J, Bettencourt C, Jayawant S, Lickiss J, Fawcett K, Clokie S, Wallis Y, Clouston P, Sims D, Houlden H, Becker EBE, Németh AH. Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44. Am J Hum Genet. 2017 Oct 05;101(4):638. doi: 10.1016/j.ajhg.2017.09.006. PMID: 28985497; PMCID: PMC5630189.
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