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

Hum Mol Genet · 2015 · PMC4614701 · PMID 26307080

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showed a trendno p-value reported

The growth curve for patient cells showed a trend of slowed initial growth which continued despite nutrient depletion ( Supplementary Material, Fig.

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