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Homozygous mutation in the eukaryotic translation initiation factor 2alpha phosphatase gene, PPP1R15B, is associated with severe microcephaly, short stature and intellectual disability. [electronic resource] by
- 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
Producer: 20160912
In:
Human molecular genetics vol. 24
Availability: No items available.
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