Enriched expression of NF1 in inhibitory neurons in both mouse and human brain

Neurofibromatosis type 1 (NF1) is an autosomal dominant disease caused by loss-of-function mutations in NF1 gene, which encodes a GTPase activating protein for RAS. NF1 affects multiple systems including brain and is highly associated with cognitive deficits such as learning difficulties and attenti...

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Detalles Bibliográficos
Autores principales: Ryu, Hyun-Hee, Kang, Minkyung, Park, Jinsil, Park, Sung-Hye, Lee, Yong-Seok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Micro Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591896/
https://www.ncbi.nlm.nih.gov/pubmed/31234911
http://dx.doi.org/10.1186/s13041-019-0481-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591896/
https://www.ncbi.nlm.nih.gov/pubmed/31234911
http://dx.doi.org/10.1186/s13041-019-0481-0

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