Publication Details

Pubmed26307080
Title: Homozygous mutation in the eukaryotic translation initiation factor 2alpha phosphatase gene, PPP1R15B, is associated with severe microcephaly, short stature and intellectual disability.
Year: 2015
DOI: https://doi.org/10.1093/hmg/ddv337
First Author: Kernohan
Experimental setup: anti bait coimmunoprecipitation (IntAct)

Interactions

1 interaction
InteractorPartnerSourcesLink
PP1G_HUMANPR15B_HUMANIntActdetails