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RELN Mutations in Autism Spectrum Disorder

RELN encodes a large, secreted glycoprotein integral to proper neuronal positioning during development and regulation of synaptic function postnatally. Rare, homozygous, null mutations lead to lissencephaly with cerebellar hypoplasia (LCH), accompanied by developmental delay and epilepsy. Until rece...

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Detalles Bibliográficos
Autores principales:	Lammert, Dawn B., Howell, Brian W.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2016
Materias:	Neuroscience
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814460/ https://www.ncbi.nlm.nih.gov/pubmed/27064498 http://dx.doi.org/10.3389/fncel.2016.00084

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