Citations for
1CDG1Y, SSR4
Expanding the Molecular and Clinical Phenotype of SSR4-CDG.
Ng BG, Raymond K, Kircher M, Buckingham KJ, Wood T, Shendure J, Nickerson DA, Bamshad MJ; University of Washington Center for Mendelian Genomics, Wong JT, Monteiro FP, Graham BH, Jackson S, Sparkes R, Scheuerle AE, Cathey S, Kok F, Gibson JB, Freeze HH.
Hum Mutat 36(11):1048-51. doi: 10.1002/humu.22856. Epub 2015 Aug 27. 2015
2CDG1Y, SSR4
A new congenital disorder of glycosylation caused by a mutation in SSR4, the signal sequence receptor 4 protein of the TRAP complex.
Losfeld ME, Ng BG, Kircher M, Buckingham KJ, Turner EH, Eroshkin A, Smith JD, Shendure J, Nickerson DA, Bamshad MJ; University of Washington Center for Mendelian Genomics, Freeze HH.
Hum Mol Genet 23(6):1602-5. doi: 10.1093/hmg/ddt550. Epub 2013 Nov 11. 2014
3SSR4
Cloning and molecular characterization of a human ortholog of Monodelphis TRAPD in ultraviolet B-induced melanoma.
Wang Z, VandeBerg JL.
Melanoma Res 14(2):107-14. 2004
4IDH3G, SSR4, PDZD4
Genomic organization of two novel genes on human Xq28: compact head to head arrangement of IDH gamma and TRAP delta is conserved in rat and mouse.
Brenner V, Nyakatura G, Rosenthal A, Platzer M.
Genomics 44(1):8-14. 1997
5SSR3, SSR4, SSR1, SSR2
A tetrameric complex of membrane proteins in the endoplasmic reticulum.
Hartmann E, Gorlich D, Kostka S, Otto A, Kraft R, Knespel S, Burger E,Rapoport TA, Prehn S.
Eur J Biochem 214(2):375-81. 1993