APA

Stevanin G., Hahn V., Lohmann E., Bouslam N., Gouttard M., Soumphonphakdy C., Welter M., Ollagnon-Roman E., Lemainque A., Ruberg M., Brice A. & Durr A. (20040907). Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14. : Archives of neurology.

Chicago

Stevanin Giovanni, Hahn Valérie, Lohmann Ebba, Bouslam Naima, Gouttard Michel, Soumphonphakdy Caroline, Welter Marie-Laure, Ollagnon-Roman Elisabeth, Lemainque Arnaud, Ruberg Merle, Brice Alexis and Durr Alexandra. 20040907. Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14. : Archives of neurology.

Harvard

Stevanin G., Hahn V., Lohmann E., Bouslam N., Gouttard M., Soumphonphakdy C., Welter M., Ollagnon-Roman E., Lemainque A., Ruberg M., Brice A. and Durr A. (20040907). Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14. : Archives of neurology.

MLA

Stevanin Giovanni, Hahn Valérie, Lohmann Ebba, Bouslam Naima, Gouttard Michel, Soumphonphakdy Caroline, Welter Marie-Laure, Ollagnon-Roman Elisabeth, Lemainque Arnaud, Ruberg Merle, Brice Alexis and Durr Alexandra. Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14. : Archives of neurology. 20040907.