P187 ZC4H2 X linked gene mutations: phenotypic spectrum of arthrogryposis multiplex congenita

Autor: Alvarenga, N., Saez, V., Lotz, S., Exposito, J., Carrera, L., Natera, D., Armijo, J., Rios, A., Artiga, V., Jou, C., Codina, A., Yubero, D., Martorell, L., Ortez, C., Nascimento, A.
Zdroj: In Neuromuscular Disorders October 2023 33 Supplement 1:S112-S112
Databáze: ScienceDirect