APA

Mollet J., Delahodde A., Serre V., Chretien D., Schlemmer D., Lombes A., Boddaert N., Desguerre I., de Lonlay P., de Baulny H. O., Munnich A. & Rötig A. (20080328). CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures. : American journal of human genetics.

Chicago

Mollet Julie, Delahodde Agnès, Serre Valérie, Chretien Dominique, Schlemmer Dimitri, Lombes Anne, Boddaert Nathalie, Desguerre Isabelle, de Lonlay Pascale, de Baulny Hélène Ogier, Munnich Arnold and Rötig Agnès. 20080328. CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures. : American journal of human genetics.

Harvard

Mollet J., Delahodde A., Serre V., Chretien D., Schlemmer D., Lombes A., Boddaert N., Desguerre I., de Lonlay P., de Baulny H. O., Munnich A. and Rötig A. (20080328). CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures. : American journal of human genetics.

MLA

Mollet Julie, Delahodde Agnès, Serre Valérie, Chretien Dominique, Schlemmer Dimitri, Lombes Anne, Boddaert Nathalie, Desguerre Isabelle, de Lonlay Pascale, de Baulny Hélène Ogier, Munnich Arnold and Rötig Agnès. CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures. : American journal of human genetics. 20080328.