Citations for
1CSMD3, DEL8P23
Two patients with balanced translocations and autistic disorder: CSMD3 as a candidate gene for autism found in their common 8q23 breakpoint area.
Floris C, Rassu S, Boccone L, Gasperini D, Cao A, Crisponi L.
Eur J Hum Genet 16(6):696-704. Epub 2008 Feb 13. 2008
2CSMD1, CSMD2, CSMD3
Identification of two new members of the CSMD gene family small star, filled.
Lau WL, Scholnick SB.
Genomics 82(3):412-5. 2003
3CSMD2,CSMD3
A novel giant gene CSMD3 encoding a protein with CUB and sushi multiple domains: a candidate gene for benign adult familial myoclonic epilepsy on human chromosome 8q23.3-q24.1.
Shimizu A, Asakawa S, Sasaki T, Yamazaki S, Yamagata H, Kudoh J, Minoshima S, Kondo I, Shimizu N.
Biochem Biophys Res Commun 309(1):143-54. 2003
4BTBD9, CCDC85A, CSMD2, CSMD3, FAM111A, FAM65A, FMNL2, GALNT13, GPRIN1, KIAA1919, KLHL32, LENG8, MIS18BP1, NEK1, PKD1L2, PNMA5, RHPN1, SCIN, SSFA2, SYNGAP1, TMEM200A, TUBGCP5, VARS2, WDR40A, ZNF45
Prediction of the coding sequences of unidentified human genes. XXI. The complete sequences of 60 new cDNA clones from brain which code for large proteins.
Nagase T, Kikuno R, Ohara O.
DNA Res 8(4):179-87. 2001