Mechanistic insights from animal models of neurofibromatosis type 1 cognitive impairment

Neurofibromatosis type 1 (NF1) is an autosomal-dominant neurogenetic disorder caused by mutations in the gene neurofibromin 1 (NF1). NF1 predisposes individuals to a variety of symptoms, including peripheral nerve tumors, brain tumors and cognitive dysfunction. Cognitive deficits can negatively impa...

Descripción completa

Detalles Bibliográficos
Autores principales: Miller, Andrew H., Halloran, Mary C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9459395/
https://www.ncbi.nlm.nih.gov/pubmed/36037004
http://dx.doi.org/10.1242/dmm.049422

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9459395/
https://www.ncbi.nlm.nih.gov/pubmed/36037004
http://dx.doi.org/10.1242/dmm.049422

Ejemplares similares