Citations for
1GNB1L
Strong evidence that GNB1L is associated with schizophrenia.
Williams NM, Glaser B, Norton N, Williams H, Pierce T, Moskvina V, Monks S, Del Favero J, Goossens D, Rujescu D, Giegling I, Kirov G, Craddock N, Murphy KC, O'Donovan MC, Owen MJ.
Hum Mol Genet 17(4):555-66. Epub 2007 Nov 13. 2008
2ARVCF, COMT, GNB1L, PRODH
Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.
Prasad SE, Howley S, Murphy KC.
Dev Disabil Res Rev 14(1):26-34. Review. 2008
3DGCR6L, GNB1L, TXNRD2
Isolation and characterization of a novel gene containing WD40 repeats from the region deleted in velo-cardio-facial/DiGeorge syndrome on chromosome 22q11.
Funke B, Pandita RK, Morrow BE.
Genomics 73(3):264-71. 2001
4GNB1L
GNB1L, a gene deleted in the critical region for DiGeorge syndrome on 22q11, encodes a G-protein beta-subunit-like polypeptide.
Gong L, Liu M, Jen J, Yeh ET.
Biochim Biophys Acta 1494(1-2):185-8. 2000