Cargando…
Identification of a Novel Nonsense Mutation in PLA2G6 and Prenatal Diagnosis in a Chinese Family With Infantile Neuroaxonal Dystrophy
BACKGROUND AND PURPOSE: Infantile neuroaxonal dystrophy (INAD) is a subtype of PLA2G6-Associated Neurodegeneration (PLAN) with an age of early onset and severe clinical phenotypes of neurodegeneration. Individuals affected with INAD are characterized by rapid progressive psychomotor deterioration, n...
Autores principales: | Zou, Yongyi, Luo, Haiyan, Yuan, Huizhen, Xie, Kang, Yang, Yan, Huang, Shuhui, Yang, Bicheng, Liu, Yanqiu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298276/ https://www.ncbi.nlm.nih.gov/pubmed/35873758 http://dx.doi.org/10.3389/fneur.2022.904027 |
Ejemplares similares
-
Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex
por: Kapoor, Saketh, et al.
Publicado: (2016) -
Novel insertion mutation in the PLA2G6 gene in an Iranian family with infantile neuroaxonal dystrophy
por: Rostampour, Dorsa, et al.
Publicado: (2022) -
Infantile neuroaxonal dystrophy caused by PLA2G6 gene mutation in a Chinese patient: A case report
por: Wang, Baotian, et al.
Publicado: (2018) -
The natural history of infantile neuroaxonal dystrophy
por: Altuame, Fadie D., et al.
Publicado: (2020) -
Catalytic Function of PLA2G6 Is Impaired by Mutations Associated with Infantile Neuroaxonal Dystrophy but Not Dystonia-Parkinsonism
por: Engel, Laura A., et al.
Publicado: (2010)