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...

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Publicat a:J Neurosci
Autors principals: Reiner, O, Albrecht, U, Gordon, M, Chianese, KA, Wong, C, Gal-Gerber, O, Sapir, T, Siracusa, LD, Buchberg, AM, Caskey, CT
Format: Artigo
Idioma:Inglês
Publicat: Society for Neuroscience 1995
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Articles
Accés en línia: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
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