APA

Lee R. G., Sedghi M., Salari M., Shearwood A. J., Stentenbach M., Kariminejad A., Goullee H., Rackham O., Laing N. G., Tajsharghi H. & Filipovska A. (2018). Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunction. : Neurology. Genetics.

Chicago

Lee Richard G, Sedghi Maryam, Salari Mehri, Shearwood Anne-Marie J, Stentenbach Maike, Kariminejad Ariana, Goullee Hayley, Rackham Oliver, Laing Nigel G, Tajsharghi Homa and Filipovska Aleksandra. 2018. Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunction. : Neurology. Genetics.

Harvard

Lee R. G., Sedghi M., Salari M., Shearwood A. J., Stentenbach M., Kariminejad A., Goullee H., Rackham O., Laing N. G., Tajsharghi H. and Filipovska A. (2018). Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunction. : Neurology. Genetics.

MLA

Lee Richard G, Sedghi Maryam, Salari Mehri, Shearwood Anne-Marie J, Stentenbach Maike, Kariminejad Ariana, Goullee Hayley, Rackham Oliver, Laing Nigel G, Tajsharghi Homa and Filipovska Aleksandra. Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunction. : Neurology. Genetics. 2018.