A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiency

por Jameel, Muhammad, Klar, Joakim, Tariq, Muhammad, Moawia, Abubakar, Altaf Malik, Naveed, Seema Waseem, Syeda, Abdullah, Uzma, Naeem Khan, Tahir, Raininko, Raili, Baig, Shahid Mahmood, Dahl, Niklas
Publicado 2014