Cargando…
Identification of an Identical de Novo SCAMP5 Missense Variant in Four Unrelated Patients With Seizures and Severe Neurodevelopmental Delay
Objective: To establish and broaden the phenotypic spectrum of secretory carrier membrane protein (SCAMP5) associated with epilepsy and neurodevelopmental delay. Methods: A Chinese patient was identified at the First Hospital of Peking University, and the three unrelated patients were recruited from...
Autores principales: | Jiao, Xianru, Morleo, Manuela, Nigro, Vincenzo, Torella, Annalaura, D’Arrigo, Stefano, Ciaccio, Claudia, Pantaleoni, Chiara, Gong, Pan, Grand, Katheryn, Sanchez-Lara, Pedro A., Krier, Joel, Fieg, Elizabeth, Stergachis, Andrew, Wang, Xiaodong, Yang, Zhixian |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7775611/ https://www.ncbi.nlm.nih.gov/pubmed/33390987 http://dx.doi.org/10.3389/fphar.2020.599191 |
Ejemplares similares
-
Children with rare diseases: do they really have an increased risk of developing epilepsy?
por: Pantaleoni, Chiara, et al.
Publicado: (2015) -
SCAMP’s stigmergic model of social conflict
por: Parunak, H. Van Dyke, et al.
Publicado: (2021) -
Case report: A novel pathogenic FRMD7 variant in a Turner syndrome patient with familial idiopathic infantile nystagmus
por: Hafdaoui, Sara, et al.
Publicado: (2023) -
Neurologic, Neuropsychologic, and Neuroradiologic Features of EBF3-Related Syndrome
por: Ciaccio, Claudia, et al.
Publicado: (2023) -
Retinal dystrophy in an individual carrying a de novo missense variant of SMARCA4
por: Cappuccio, Gerarda, et al.
Publicado: (2019)