APA
Watson L. M., Bamber E., Schnekenberg R. P., Williams J., Bettencourt C., Lickiss J., Jayawant S., Fawcett K., Clokie S., Wallis Y., Clouston P., Sims D., Houlden H., Becker E. B. E. & Németh A. H. (112017). Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44. : American journal of human genetics.
Chicago
Watson Lauren M, Bamber Elizabeth, Schnekenberg Ricardo Parolin, Williams Jonathan, Bettencourt Conceição, Lickiss Jennifer, Jayawant Sandeep, Fawcett Katherine, Clokie Samuel, Wallis Yvonne, Clouston Penny, Sims David, Houlden Henry, Becker Esther B E and Németh Andrea H. 112017. Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44. : American journal of human genetics.
Harvard
Watson L. M., Bamber E., Schnekenberg R. P., Williams J., Bettencourt C., Lickiss J., Jayawant S., Fawcett K., Clokie S., Wallis Y., Clouston P., Sims D., Houlden H., Becker E. B. E. and Németh A. H. (112017). Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44. : American journal of human genetics.
MLA
Watson Lauren M, Bamber Elizabeth, Schnekenberg Ricardo Parolin, Williams Jonathan, Bettencourt Conceição, Lickiss Jennifer, Jayawant Sandeep, Fawcett Katherine, Clokie Samuel, Wallis Yvonne, Clouston Penny, Sims David, Houlden Henry, Becker Esther B E and Németh Andrea H. Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44. : American journal of human genetics. 112017.