Neurotransmitters and Sodium Channelopathies; Possible Link?

Investigators from the University of British Columbia, Great Ormond Street Hospital for Children, and the National Hospital reported their findings on neurotransmitter deficiencies in two patients with mutations in voltage-gated sodium genes (SCN2A and SCN8A) discovered by whole exome sequencing.

Detalles Bibliográficos
Autores principales: Hammer, Michael F., Encinas, Alejandra D.C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pediatric Neurology Briefs Publishers 2017
Materias:
Genetic Disorders
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681457/
https://www.ncbi.nlm.nih.gov/pubmed/29184379
http://dx.doi.org/10.15844/pedneurbriefs-31-3-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681457/
https://www.ncbi.nlm.nih.gov/pubmed/29184379
http://dx.doi.org/10.15844/pedneurbriefs-31-3-1

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