Cargando...
Lissencephaly gene (LIS1) expression in the CNS suggests a role in neuronal migration
Miller-Dieker lissencephaly syndrome (MDS) is a human developmental brain malformation caused by neuronal migration defects resulting in abnormal layering of the cerebral cortex. LIS1, the gene defective in MDS, encodes a subunit of brain platelet-activating factor (PAF) acetylhydrolase which inacti...
Gardado en:
| Publicado en: | J Neurosci |
|---|---|
| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Society for Neuroscience
1995
|
| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6578245/ https://ncbi.nlm.nih.gov/pubmed/7751941 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.15-05-03730.1995 |
| Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|