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. |
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Zdroj: | In Neuromuscular Disorders October 2023 33 Supplement 1:S112-S112 |
Databáze: | ScienceDirect |
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