Cargando…
Whole exome sequencing identifies a rare variant in MAS1 gene in a subject with lethal COVID-19
COVID-19 may be considered a multifactorial disease caused by the interaction between the virus itself, as the environmental contribute, and the genetic background of the host. SARS-CoV-2 infection occurs through the interaction between the spike protein and ACE2, a receptor in the host cells. Clini...
Autores principales: | Azzarà, Alessia, Cassano, Ilaria, Tirindelli, Maria Cristina, Nobile, Carolina, Schittone, Valentina, Paccagnella, Elisa, Lintas, Carla, Gurrieri, Fiorella |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors. Published by Elsevier Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633625/ https://www.ncbi.nlm.nih.gov/pubmed/36348959 http://dx.doi.org/10.1016/j.genrep.2022.101705 |
Ejemplares similares
-
Genetic variants determine intrafamilial variability of SARS-CoV-2 clinical outcomes in 19 Italian families
por: Azzarà, Alessia, et al.
Publicado: (2022) -
Genetic Characterization in Familial Rotator Cuff Tear: An Exome Sequencing Study
por: Azzarà, Alessia, et al.
Publicado: (2022) -
Genotype–Phenotype Correlations in Relation to Newly Emerging Monogenic Forms of Autism Spectrum Disorder and Associated Neurodevelopmental Disorders: The Importance of Phenotype Reevaluation after Pangenomic Results
por: Lintas, Carla, et al.
Publicado: (2021) -
Genetic Dysruption of the Histaminergic Pathways: A Novel Deletion at the 15q21.2 locus Associated with Variable Expressivity of Neuropsychiatric Disorders
por: Lintas, Carla, et al.
Publicado: (2022) -
Deletion of a Single Lysine Residue at Position 292 of CAMK2A Disrupts Protein Function, Causing Severe Epileptic Encephalopathy and Intellectual Disability
por: Lintas, Carla, et al.
Publicado: (2023)