APA

Kernohan K. D., Cigana Schenkel L., Huang L., Smith A., Pare G., Ainsworth P., Boycott K. M., Warman-Chardon J. & Sadikovic B. (20170428). Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy. : Clinical epigenetics.

Chicago

Kernohan Kristin D, Cigana Schenkel Laila, Huang Lijia, Smith Amanda, Pare Guillaume, Ainsworth Peter, Boycott Kym M, Warman-Chardon Jodi and Sadikovic Bekim. 20170428. Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy. : Clinical epigenetics.

Harvard

Kernohan K. D., Cigana Schenkel L., Huang L., Smith A., Pare G., Ainsworth P., Boycott K. M., Warman-Chardon J. and Sadikovic B. (20170428). Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy. : Clinical epigenetics.

MLA

Kernohan Kristin D, Cigana Schenkel Laila, Huang Lijia, Smith Amanda, Pare Guillaume, Ainsworth Peter, Boycott Kym M, Warman-Chardon Jodi and Sadikovic Bekim. Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy. : Clinical epigenetics. 20170428.