A Specific Diplotype H1j/H2 of the MAPT Gene Could Be Responsible for Parkinson's Disease with Dementia

por Smaili, Imane, Hajjaj, Imane, Razine, Rachid, Tibar, Houyam, Salmi, Ayyoub, Bouslam, Naima, Moussa, Ahmed, Regragui, Wafa, Bouhouche, Ahmed
Publicado 2020

Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing

por Bouhouche, Ahmed, Tibar, Houyam, Kriouale, Yamna, Jiddane, Mohammed, Smaili, Imane, Bouslam, Naima, Benomar, Ali, Yahyaoui, Mohamed, El Fahime, Elmostafa
Publicado 2018

Novel pathogenic VPS13A mutation in Moroccan family with Choreoacanthocytosis: a case report

por Ouchkat, Fatima, Regragui, Wafaa, Smaili, Imane, Naciri Darai, Hajar, Bouslam, Naima, Rahmani, Mounia, Melhaoui, Adyl, Arkha, Yasser, El Fahime, Elmostafa, Bouhouche, Ahmed
Publicado 2020