Homozygous mutation in the eukaryotic translation initiation factor 2alpha phosphatase gene, PPP1R15B, is associated with severe microcephaly, short stature and intellectual disability

Protein translation is an essential cellular process initiated by the association of a methionyl–tRNA with the translation initiation factor eIF2. The Met-tRNA/eIF2 complex then associates with the small ribosomal subunit, other translation factors and mRNA, which together comprise the translational...

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Detalles Bibliográficos
Autores principales: Kernohan, Kristin D., Tétreault, Martine, Liwak-Muir, Urszula, Geraghty, Michael T., Qin, Wen, Venkateswaran, Sunita, Davila, Jorge, Holcik, Martin, Majewski, Jacek, Richer, Julie, Boycott, Kym M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614701/
https://www.ncbi.nlm.nih.gov/pubmed/26307080
http://dx.doi.org/10.1093/hmg/ddv337

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614701/
https://www.ncbi.nlm.nih.gov/pubmed/26307080
http://dx.doi.org/10.1093/hmg/ddv337

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