Genetic association signal near NTN4 in Tourette Syndrome

Tourette Syndrome (TS) is a neurodevelopmental disorder with a complex genetic etiology. Through an international collaboration, we genotyped 42 single nucleotide polymorphisms (SNPs)(p<10(−3)) from the recent TS genome-wide association study (GWAS) in 609 independent cases and 610 ancestry-match...

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Detalhes bibliográficos
Main Authors: Paschou, Peristera, Yu, Dongmei, Gerber, Gloria, Evans, Patrick, Tsetsos, Fotis, Davis, Lea K., Karagiannidis, Iordanis, Chaponis, Jonathan, Gamazon, Eric, Mueller-Vahl, Kirsten, Stuhrmann, Manfred, Schloegelhofer, Monika, Stamenkovic, Mara, Hebebrand, Johannes, Noethen, Markus, Nagy, Peter, Barta, Csaba, Tarnok, Zsanett, Rizzo, Renata, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Cath, Danielle C., Budman, Cathy L., Sandor, Paul, Barr, Cathy, Wolanczyk, Thomas, Singer, Harvey, Chou, I-Ching, Grados, Marco, Posthuma, Danielle, Rouleau, Guy A., Aschauer, Harald, Freimer, Nelson B., Pauls, David L., Cox, Nancy J., Mathews, Carol A., Scharf, Jeremiah M.
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4140987/
https://ncbi.nlm.nih.gov/pubmed/25042818
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.24215
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