Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability
Titel:
Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability
Auteur:
Law, Rosalind Dixon-Salazar, Tracy Jerber, Julie Cai, Na Abbasi, Ansar A. Zaki, Maha S. Mittal, Kirti Gabriel, Stacey B. Rafiq, Muhammad Arshad Khan, Valeed Nguyen, Maria Ali, Ghazanfar Copeland, Brett Scott, Eric Vasli, Nasim Mikhailov, Anna Khan, Muhammad Nasim Andrade, Danielle M. Ayaz, Muhammad Ansar, Muhammad Ayub, Muhammad Vincent, John B. Gleeson, Joseph G.