APA
Lesage S., Patin E., Condroyer C., Leutenegger A., Lohmann E., Giladi N., Bar-Shira A., Belarbi S., Hecham N., Pollak P., Ouvrard-Hernandez A., Bardien S., Carr J., Benhassine T., Tomiyama H., Pirkevi C., Hamadouche T., Cazeneuve C., Basak A. N., Hattori N., Dürr A., Tazir M., Orr-Urtreger A., Quintana-Murci L. & Brice A. (20100721). Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans. : Human molecular genetics.
Chicago
Lesage Suzanne, Patin Etienne, Condroyer Christel, Leutenegger Anne-Louise, Lohmann Ebba, Giladi Nir, Bar-Shira Anat, Belarbi Soraya, Hecham Nassima, Pollak Pierre, Ouvrard-Hernandez Anne-Marie, Bardien Soraya, Carr Jonathan, Benhassine Traki, Tomiyama Hiroyuki, Pirkevi Caroline, Hamadouche Tarik, Cazeneuve Cécile, Basak A Nazli, Hattori Nobutaka, Dürr Alexandra, Tazir Meriem, Orr-Urtreger Avi, Quintana-Murci Lluis and Brice Alexis. 20100721. Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans. : Human molecular genetics.
Harvard
Lesage S., Patin E., Condroyer C., Leutenegger A., Lohmann E., Giladi N., Bar-Shira A., Belarbi S., Hecham N., Pollak P., Ouvrard-Hernandez A., Bardien S., Carr J., Benhassine T., Tomiyama H., Pirkevi C., Hamadouche T., Cazeneuve C., Basak A. N., Hattori N., Dürr A., Tazir M., Orr-Urtreger A., Quintana-Murci L. and Brice A. (20100721). Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans. : Human molecular genetics.
MLA
Lesage Suzanne, Patin Etienne, Condroyer Christel, Leutenegger Anne-Louise, Lohmann Ebba, Giladi Nir, Bar-Shira Anat, Belarbi Soraya, Hecham Nassima, Pollak Pierre, Ouvrard-Hernandez Anne-Marie, Bardien Soraya, Carr Jonathan, Benhassine Traki, Tomiyama Hiroyuki, Pirkevi Caroline, Hamadouche Tarik, Cazeneuve Cécile, Basak A Nazli, Hattori Nobutaka, Dürr Alexandra, Tazir Meriem, Orr-Urtreger Avi, Quintana-Murci Lluis and Brice Alexis. Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans. : Human molecular genetics. 20100721.