APA

Gerards M., Sluiter W., van den Bosch B. J. C., de Wit L. E. A., Calis C. M. H., Frentzen M., Akbari H., Schoonderwoerd K., Scholte H. R., Jongbloed R. J., Hendrickx A. T. M., de Coo I. F. M. & Smeets H. J. M. (20101124). Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome. : Journal of medical genetics.

Chicago

Gerards M, Sluiter W, van den Bosch B J C, de Wit L E A, Calis C M H, Frentzen M, Akbari H, Schoonderwoerd K, Scholte H R, Jongbloed R J, Hendrickx A T M, de Coo I F M and Smeets H J M. 20101124. Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome. : Journal of medical genetics.

Harvard

Gerards M., Sluiter W., van den Bosch B. J. C., de Wit L. E. A., Calis C. M. H., Frentzen M., Akbari H., Schoonderwoerd K., Scholte H. R., Jongbloed R. J., Hendrickx A. T. M., de Coo I. F. M. and Smeets H. J. M. (20101124). Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome. : Journal of medical genetics.

MLA

Gerards M, Sluiter W, van den Bosch B J C, de Wit L E A, Calis C M H, Frentzen M, Akbari H, Schoonderwoerd K, Scholte H R, Jongbloed R J, Hendrickx A T M, de Coo I F M and Smeets H J M. Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome. : Journal of medical genetics. 20101124.