Kernohan, K. D., Tétreault, M., Liwak-Muir, U., Geraghty, M. T., Qin, W., Venkateswaran, S., . . . Boycott, K. M. (2015). 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.
Styl cytowania ChicagoKernohan, Kristin D., et al. "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.
Styl cytowania MLAKernohan, Kristin D., et al. "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.