Anzahl der Einträge: 2.
2020
Lessel, Davor ![ORCID 0000-0003-4496-244X](/images/orcid_16x16.gif)
,
Zeitler, Daniela M.,
Reijnders, Margot R. F.,
Kazantsev, Andriy,
Hassani Nia, Fatemeh,
Bartholomäus, Alexander,
Martens, Victoria,
Bruckmann, Astrid,
Graus, Veronika,
McConkie-Rosell, Allyn,
McDonald, Marie,
Lozic, Bernarda,
Tan, Ee-Shien,
Gerkes, Erica,
Johannsen, Jessika,
Denecke, Jonas,
Telegrafi, Aida,
Zonneveld-Huijssoon, Evelien,
Lemmink, Henny H.,
Cham, Breana W. M.,
Kovacevic, Tanja,
Ramsdell, Linda,
Foss, Kimberly,
Le Duc, Diana,
Mitter, Diana,
Syrbe, Steffen,
Merkenschlager, Andreas,
Sinnema, Margje,
Panis, Bianca,
Lazier, Joanna,
Osmond, Matthew,
Hartley, Taila,
Mortreux, Jeremie,
Busa, Tiffany,
Missirian, Chantal,
Prasun, Pankaj,
Lüttgen, Sabine,
Mannucci, Ilaria,
Lessel, Ivana ![ORCID 0000-0003-4496-244X](/images/orcid_16x16.gif)
,
Schob, Claudia,
Kindler, Stefan,
Pappas, John ![ORCID 0000-0001-5625-2598](/images/orcid_16x16.gif)
,
Rabin, Rachel,
Willemsen, Marjolein,
Gardeitchik, Thatjana,
Löhner, Katharina,
Rump, Patrick,
Dias, Kerith-Rae,
Evans, Carey-Anne,
Andrews, Peter Ian,
Roscioli, Tony,
Brunner, Han G.,
Chijiwa, Chieko,
Lewis, M. E. Suzanne ![ORCID 0000-0002-6300-5381](/images/orcid_16x16.gif)
,
Jamra, Rami Abou,
Dyment, David A.,
Boycott, Kym M.,
Stegmann, Alexander P. A.,
Kubisch, Christian,
Tan, Ene-Choo,
Mirzaa, Ghayda M.,
McWalter, Kirsty,
Kleefstra, Tjitske,
Pfundt, Rolph,
Ignatova, Zoya,
Meister, Gunter und
Kreienkamp, Hans-Jürgen
(2020)
Germline AGO2 mutations impair RNA interference and human neurological development.
Nature Communications 11 (1).
Volltext nicht vorhanden.
Zech, Michael,
Jech, Robert,
Boesch, Sylvia,
Škorvánek, Matej,
Weber, Sandrina,
Wagner, Matias,
Zhao, Chen,
Jochim, Angela,
Necpál, Ján,
Dincer, Yasemin,
Vill, Katharina,
Distelmaier, Felix,
Stoklosa, Malgorzata,
Krenn, Martin,
Grunwald, Stephan ![ORCID 0000-0003-3978-6277](/images/orcid_16x16.gif)
,
Bock-Bierbaum, Tobias,
Fečíková, Anna,
Havránková, Petra,
Roth, Jan,
Příhodová, Iva,
Adamovičová, Miriam,
Ulmanová, Olga,
Bechyně, Karel,
Danhofer, Pavlína,
Veselý, Branislav,
Haň, Vladimír,
Pavelekova, Petra,
Gdovinová, Zuzana,
Mantel, Tobias,
Meindl, Tobias,
Sitzberger, Alexandra,
Schröder, Sebastian,
Blaschek, Astrid,
Roser, Timo,
Bonfert, Michaela V.,
Haberlandt, Edda,
Plecko, Barbara,
Leineweber, Birgit,
Berweck, Steffen,
Herberhold, Thomas,
Langguth, Berthold,
Švantnerová, Jana,
Minár, Michal,
Ramos-Rivera, Gonzalo Alonso,
Wojcik, Monica H.,
Pajusalu, Sander,
Õunap, Katrin,
Schatz, Ulrich A.,
Pölsler, Laura,
Milenkovic, Ivan ![ORCID 0000-0002-2990-0243](/images/orcid_16x16.gif)
,
Laccone, Franco,
Pilshofer, Veronika,
Colombo, Roberto,
Patzer, Steffi,
Iuso, Arcangela,
Vera, Julia,
Troncoso, Monica,
Fang, Fang,
Prokisch, Holger,
Wilbert, Friederike,
Eckenweiler, Matthias,
Graf, Elisabeth,
Westphal, Dominik S.,
Riedhammer, Korbinian M.,
Brunet, Theresa,
Alhaddad, Bader,
Berutti, Riccardo,
Strom, Tim M.,
Hecht, Martin,
Baumann, Matthias,
Wolf, Marc,
Telegrafi, Aida,
Person, Richard E.,
Zamora, Francisca Millan,
Henderson, Lindsay B.,
Weise, David,
Musacchio, Thomas,
Volkmann, Jens,
Szuto, Anna,
Becker, Jessica,
Cremer, Kirsten,
Sycha, Thomas,
Zimprich, Fritz,
Kraus, Verena,
Makowski, Christine,
Gonzalez-Alegre, Pedro,
Bardakjian, Tanya M.,
Ozelius, Laurie J.,
Vetro, Annalisa,
Guerrini, Renzo ![ORCID 0000-0002-7272-7079](/images/orcid_16x16.gif)
,
Maier, Esther,
Borggraefe, Ingo,
Kuster, Alice,
Wortmann, Saskia B.,
Hackenberg, Annette,
Steinfeld, Robert,
Assmann, Birgit,
Staufner, Christian,
Opladen, Thomas,
Růžička, Evžen,
Cohn, Ronald D.,
Dyment, David,
Chung, Wendy K.,
Engels, Hartmut,
Ceballos-Baumann, Andres,
Ploski, Rafal,
Daumke, Oliver,
Haslinger, Bernhard,
Mall, Volker,
Oexle, Konrad und
Winkelmann, Juliane
(2020)
Monogenic variants in dystonia: an exome-wide sequencing study.
The Lancet Neurology 19 (11), S. 908-918.
Volltext nicht vorhanden.
Diese Liste wurde erzeugt am Fri Aug 16 07:11:48 2024 CEST.