Number of items: 2.
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Giri, Anamika, Mok, Kin Y ORCID: 0000-0003-3145-880X, Jansen, Iris, Sharma, Manu, Tesson, Christelle, Mangone, Graziella ORCID: 0000-0002-2847-3067, Lesage, Suzanne, Bras, José M ORCID: 0000-0001-8186-0333, Shulman, Joshua M, Sheerin, Una-Marie et al (show 15 more authors) , International Parkinson's Disease Consortium (IPDGC), , Díez-Fairen, Mónica ORCID: 0000-0003-1882-0309, Pastor, Pau ORCID: 0000-0002-7493-8777, Martí, María José, Ezquerra, Mario ORCID: 0000-0003-3246-6641, Tolosa, Eduardo, Correia-Guedes, Leonor ORCID: 0000-0002-8422-0494, Ferreira, Joaquim, Amin, Najaf ORCID: 0000-0002-8944-1771, van Duijn, Cornelia M ORCID: 0000-0002-2374-9204, van Rooij, Jeroen, Uitterlinden, André G ORCID: 0000-0002-7276-3387, Kraaij, Robert, Nalls, Michael and Simón-Sánchez, Javier ORCID: 0000-0001-5141-5829
(2017)
Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian population.
Neurobiology of aging, 50.
167.e11-167.e13.
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May, Patrick, Girard, Simon, Harrer, Merle, Bobbili, Dheeraj R, Schubert, Julian, Wolking, Stefan, Becker, Felicitas, Lachance-Touchette, Pamela, Meloche, Caroline, Gravel, Micheline et al (show 88 more authors) , Niturad, Cristina E, Knaus, Julia, De Kovel, Carolien, Toliat, Mohamad, Polvi, Anne, Iacomino, Michele, Guerrero-Lopez, Rosa, Baulac, Stephanie, Marini, Carla, Thiele, Holger, Altmueller, Janine, Jabbari, Kamel, Ruppert, Ann-Kathrin, Jurkowski, Wiktor, Lal, Dennis, Rusconi, Raffaella, Cestele, Sandrine, Terragni, Benedetta, Coombs, Ian D, Reid, Christopher A, Striano, Pasquale, Caglayan, Hande, Siren, Auli, Everett, Kate, Moller, Rikke S, Hjalgrim, Helle, Muhle, Hiltrud, Helbig, Ingo, Kunz, Wolfram S, Weber, Yvonne G, Weckhuysen, Sarah, De Jonghe, Peter, Sisodiya, Sanjay M, Nabbout, Rima, Franceschetti, Silvana, Coppola, Antonietta, Vari, Maria S, Trenite, Dorothee Kasteleijn-Nolst, Baykan, Betul, Ozbek, Ugur, Bebek, Nerses, Klein, Karl M, Rosenow, Felix, Nguyen, Dang K, Dubeau, Francois, Carmant, Lionel, Lortie, Anne, Desbiens, Richard, Clement, Jean-Francois, Cieuta-Walti, Cecile, Sills, Graeme J ORCID: 0000-0002-3389-8713, Auce, Pauls, Francis, Ben ORCID: 0000-0002-2130-5976, Johnson, Michael R, Marson, Anthony G ORCID: 0000-0002-6861-8806, Berghuis, Bianca, Sander, Josemir W, Avbersek, Andreja, McCormack, Mark, Cavalleri, Gianpiero L, Delanty, Norman, Depondt, Chantal, Krenn, Martin, Zimprich, Fritz, Peter, Sarah, Nikanorova, Marina, Kraaij, Robert, van Rooij, Jeroen, Balling, Rudi, Ikram, M Arfan, Uitterlinden, Andre G, Avanzini, Giuliano, Schorge, Stephanie, Petrou, Steven, Mantegazza, Massimo, Sander, Thomas, LeGuern, Eric, Serratosa, Jose M, Koeleman, Bobby PC, Palotie, Aarno, Lehesjoki, Anna-Elina, Nothnagel, Michael, Nuernberg, Peter, Maljevic, Snezana, Zara, Federico, Cossette, Patrick, Krause, Roland and Lerche, Holger
(2018)
Rare coding variants in genes encoding GABA<sub>A</sub> receptors in genetic generalised epilepsies: an exome-based case-control study.
LANCET NEUROLOGY, 17 (8).
pp. 699-708.
This list was generated on Sun Mar 17 19:42:17 2024 GMT.