Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly.
DiStasio A, Driver A, Sund K, Donlin M, Muraleedharan RM, Pooya S, Kline-Fath B, Kaufman KM, Prows CA, Schorry E, Dasgupta B, Stottmann RW.
DiStasio A, et al. Among authors: donlin m.
Hum Mol Genet. 2017 Dec 15;26(24):4836-4848. doi: 10.1093/hmg/ddx362.
Hum Mol Genet. 2017.
PMID: 29036432
Free PMC article.