Gene Review:
IMMP2L - IMP2 inner mitochondrial membrane...
Homo sapiens
Synonyms:
IMMP2L-IT1, IMP2, IMP2-LIKE, IMP2-like protein, Mitochondrial inner membrane protease subunit 2
- Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome. Petek, E., Windpassinger, C., Vincent, J.B., Cheung, J., Boright, A.P., Scherer, S.W., Kroisel, P.M., Wagner, K. Am. J. Hum. Genet. (2001)
- 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, M.M., Aschauer, H.N., Gurling, H.M., Kroisel, P.M., Wagner, K., Scherer, S.W., Vincent, J.B. Mol. Genet. Genomics (2007)
- Association between 7q31 markers and Tourette syndrome. Díaz-Anzaldúa, A., Joober, R., Rivière, J.B., Dion, Y., Lespérance, P., Chouinard, S., Richer, F., Rouleau, G.A. Am. J. Med. Genet. A (2004)