Cargando…
CNNM2 Mutations Cause Impaired Brain Development and Seizures in Patients with Hypomagnesemia
Intellectual disability and seizures are frequently associated with hypomagnesemia and have an important genetic component. However, to find the genetic origin of intellectual disability and seizures often remains challenging because of considerable genetic heterogeneity and clinical variability. In...
Autores principales: | Arjona, Francisco J., de Baaij, Jeroen H. F., Schlingmann, Karl P., Lameris, Anke L. L., van Wijk, Erwin, Flik, Gert, Regele, Sabrina, Korenke, G. Christoph, Neophytou, Birgit, Rust, Stephan, Reintjes, Nadine, Konrad, Martin, Bindels, René J. M., Hoenderop, Joost G. J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974678/ https://www.ncbi.nlm.nih.gov/pubmed/24699222 http://dx.doi.org/10.1371/journal.pgen.1004267 |
Ejemplares similares
-
Novel CNNM2 Mutation Responsible for Autosomal-Dominant Hypomagnesemia With Seizure
por: Tseng, Min-Hua, et al.
Publicado: (2022) -
Diabetes-induced hypomagnesemia is not modulated by metformin treatment in mice
por: Kurstjens, Steef, et al.
Publicado: (2019) -
Mechanisms of proton pump inhibitor‐induced hypomagnesemia
por: Gommers, Lisanne M. M., et al.
Publicado: (2022) -
Novel variant in the CNNM2 gene associated with dominant hypomagnesemia
por: García-Castaño, Alejandro, et al.
Publicado: (2020) -
The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2)
por: Franken, Gijs A. C., et al.
Publicado: (2021)