Citations for
1GTS7, IMMP2L
Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome.
Patel C, Cooper-Charles L, McMullan DJ, Walker JM, Davison V, Morton J.
Eur J Hum Genet 19(6):634-9. Epub 2011 Mar 9. 2011
2GTS7, IMMP2L
Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome.
Patel C, Cooper-Charles L, McMullan DJ, Walker JM, Davison V, Morton J.
Eur J Hum Genet 19(6):634-9. Epub 2011 Mar 9. 2011
3FER1L6, IMMP2L, MEIG1
Copy number variants in premature ovarian failure and ovarian dysgenesis.
Ledig S, Röpke A, Wieacker P.
Sex Dev 4(4-5):225-32. Epub 2010 Jul 3. 2010
4GTS7, IMMP2L
Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome.
Petek E, Schwarzbraun T, Noor A, Patel M, Nakabayashi K, Choufani S, Windpassinger C, Stamenkovic M, Robertson MM, Aschauer HN, Gurling HM, Kroisel PM, Wagner K, Scherer SW, Vincent JB.
Mol Genet Genomics 277(1):71-81. Epub 2006 Oct 17. 2007
5GTS7, IMMP2L
Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome.
Petek E, Windpassinger C, Vincent JB, Cheung J, Boright AP, Scherer SW, Kroisel PM, Wagner K.
Am J Hum Genet 68(4):848-58. Epub 2001 Mar 9. 2001
6GTS7, IMMP2L
Candidate region for Gilles de la Tourette syndrome at 7q31.
Kroisel PM, Petek E, Emberger W, Windpassinger C, Wladika W, Wagner K.
Am J Med Genet 101(3):259-61. 2001