APA

Ferrier A., Sato T., De Repentigny Y., Gibeault S., Bhanot K., O'Meara R. W., Lynch-Godrei A., Kornfeld S. F., Young K. G. & Kothary R. (20141203). Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI. : Human molecular genetics.

Chicago

Ferrier Andrew, Sato Tadasu, De Repentigny Yves, Gibeault Sabrina, Bhanot Kunal, O'Meara Ryan W, Lynch-Godrei Anisha, Kornfeld Samantha F, Young Kevin G and Kothary Rashmi. 20141203. Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI. : Human molecular genetics.

Harvard

Ferrier A., Sato T., De Repentigny Y., Gibeault S., Bhanot K., O'Meara R. W., Lynch-Godrei A., Kornfeld S. F., Young K. G. and Kothary R. (20141203). Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI. : Human molecular genetics.

MLA

Ferrier Andrew, Sato Tadasu, De Repentigny Yves, Gibeault Sabrina, Bhanot Kunal, O'Meara Ryan W, Lynch-Godrei Anisha, Kornfeld Samantha F, Young Kevin G and Kothary Rashmi. Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI. : Human molecular genetics. 20141203.