
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
LINGO2
Introduction
Leucine rich repeat and Ig domain containing 2 is a protein that in humans is encoded by the LINGO2 gene. [1]
References
References
- ↑ “Entrez Gene: Leucine rich repeat and Ig domain containing 2”. Retrieved 2014-03-31.
Further reading
Further reading
- Ferreira, R. C.; Pan-Hammarström, Q; Graham, R. R.; Gateva, V; Fontán, G; Lee, A. T.; Ortmann, W; Urcelay, E; Fernández-Arquero, M; Núñez, C; Jorgensen, G; Ludviksson, B. R.; Koskinen, S; Haimila, K; Clark, H. F.; Klareskog, L; Gregersen, P. K.; Behrens, T. W.; Hammarström, L (2010). “Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency”. Nature Genetics. 42 (9): 777–80. doi:10.1038/ng.644. PMID 20694011.
- Wu, Y. W.; Prakash, K. M.; Rong, T. Y.; Li, H. H.; Xiao, Q; Tan, L. C.; Au, W. L.; Ding, J. Q.; Chen, S. D.; Tan, E. K. (2011). “Lingo2 variants associated with essential tremor and Parkinson’s disease”. Human Genetics. 129 (6): 611–5. doi:10.1007/s00439-011-0955-3. PMID 21287203.
- Su, F. C.; Chen, C. M.; Chen, Y. C.; Wu, Y. R. (2012). “LINGO-2 polymorphism and the risk of Parkinson’s disease in Taiwan”. Parkinsonism & Related Disorders. 18 (5): 609–11. doi:10.1016/j.parkreldis.2011.11.013. PMID 22123311.
- Ichikawa, S; Koller, D. L.; Padgett, L. R.; Lai, D; Hui, S. L.; Peacock, M; Foroud, T; Econs, M. J. (2010). “Replication of previous genome-wide association studies of bone mineral density in premenopausal American women”. Journal of Bone and Mineral Research. 25 (8): 1821–9. doi:10.1002/jbmr.62. PMC 3153352. PMID 20200978.
- Vilariño-Güell, C; Wider, C; Ross, O. A.; Jasinska-Myga, B; Kachergus, J; Cobb, S. A.; Soto-Ortolaza, A. I.; Behrouz, B; Heckman, M. G.; Diehl, N. N.; Testa, C. M.; Wszolek, Z. K.; Uitti, R. J.; Jankovic, J; Louis, E. D.; Clark, L. N.; Rajput, A; Farrer, M. J. (2010). “LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease”. Neurogenetics. 11 (4): 401–8. doi:10.1007/s10048-010-0241-x. PMC 3930084. PMID 20369371.
- Carim-Todd, L; Escarceller, M; Estivill, X; Sumoy, L (2003). “LRRN6A/LERN1 (leucine-rich repeat neuronal protein 1), a novel gene with enriched expression in limbic system and neocortex”. The European Journal of Neuroscience. 18 (12): 3167–82. doi:10.1111/j.1460-9568.2003.03003.x. PMID 14686891.
- Speliotes, E. K.; Willer, C. J.; Berndt, S. I.; Monda, K. L.; Thorleifsson, G; Jackson, A. U.; Lango Allen, H; Lindgren, C. M.; Luan, J; Mägi, R; Randall, J. C.; Vedantam, S; Winkler, T. W.; Qi, L; Workalemahu, T; Heid, I. M.; Steinthorsdottir, V; Stringham, H. M.; Weedon, M. N.; Wheeler, E; Wood, A. R.; Ferreira, T; Weyant, R. J.; Segrè, A. V.; Estrada, K; Liang, L; Nemesh, J; Park, J. H.; Gustafsson, S; Kilpeläinen, T. O. (2010). “Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index”. Nature Genetics. 42 (11): 937–48. doi:10.1038/ng.686. PMC 3014648. PMID 20935630.
