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SIL1, a causative cochaperone gene of Marinesco-Sjögren syndrome, plays an essential role in establishing the architecture of the developing cerebral cortex
Marinesco-Sjögren syndrome (MSS) is a rare autosomal recessively inherited disorder with mental retardation (MR). Recently, mutations in the SIL1 gene, encoding a co-chaperone which regulates the chaperone HSPA5, were identified as a major cause of MSS. We here examined the pathophysiological signif...
Autores principales: | Inaguma, Yutaka, Hamada, Nanako, Tabata, Hidenori, Iwamoto, Ikuko, Mizuno, Makoto, Nishimura, Yoshiaki V, Ito, Hidenori, Morishita, Rika, Suzuki, Motomasa, Ohno, Kinji, Kumagai, Toshiyuki, Nagata, Koh-ichi |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958314/ https://www.ncbi.nlm.nih.gov/pubmed/24473200 http://dx.doi.org/10.1002/emmm.201303069 |
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