Cargando…
Exonic deletion of SLC9A9 in autism with epilepsy
Autores principales: | Cardon, Meeta, Evankovich, Karen D., Holder, J. Lloyd |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830193/ https://www.ncbi.nlm.nih.gov/pubmed/27123481 http://dx.doi.org/10.1212/NXG.0000000000000062 |
Ejemplares similares
-
A 3.9-Mb Deletion on 2p11.2 Comprising the REEP1 Gene Causes Early-Onset Atypical Parkinsonism
por: Baviera-Muñoz, Raquel, et al.
Publicado: (2021) -
Anti-Hu limbic encephalitis preceding the appearance of mediastinal germinoma by 9 years
por: Silsby, Matthew, et al.
Publicado: (2020) -
Null mutation in SCN9A in which noxious stimuli can be detected in the absence of pain
por: Ramirez, Juan D., et al.
Publicado: (2014) -
Erythromelalgia: A Child With V400M Mutation in the SCN9A Gene
por: Nwebube, Chineze, et al.
Publicado: (2021) -
Ataxia-Pancytopenia Syndrome due to a de Novo SAMD9L Mutation
por: King-Robson, Josh, et al.
Publicado: (2021)