Citations for
1ISPD, TMEM5, WLKWS1, WLKWS2, WLKWS3, WLKWS4, WLKWS5, WLKWS7, WLKWS8
Identification of Mutations in TMEM5 and ISPD as a Cause of Severe Cobblestone Lissencephaly.
Vuillaumier-Barrot S, Bouchet-Séraphin C, Chelbi M, Devisme L, Quentin S, Gazal S, Laquerrière A, Fallet-Bianco C, Loget P, Odent S, Carles D, Bazin A, Aziza J, Clemenson A, Guimiot F, Bonnière M, Monnot S, Bole-Feysot C, Bernard JP, Loeuillet L, Gonzales M, Socha K, Grandchamp B, Attié-Bitach T, Encha-Razavi F, Seta N.
Am J Hum Genet 91(6):1135-43. doi: 10.1016/j.ajhg.2012.10.009. 2012
2B3GNT3, RARRES2, CNPY2, TMEM5
Selection of cDNAs encoding putative type II membrane proteins on the cell surface from a human full-length cDNA bank.
Yokoyama-Kobayashi M, Yamaguchi T, Sekine S, Kato S.
Gene 228(1-2):161-7. 1999