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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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| Pubblicato in: | Front Cell Neurosci |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Frontiers Media S.A.
2016
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4814460/ https://ncbi.nlm.nih.gov/pubmed/27064498 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2016.00084 |
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