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1 Ergebnisse
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Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exo..:
Collaborative, Epi25
;
Feng, Yen-Chen Anne
;
Howrigan, Daniel P
...
qt0wz3s560. , 2019
Link:
https://escholarship.org/uc/item/0wz3s560
RT Journal T1
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt0wz3s560&Exemplar=1&LAN=DE A1 Collaborative, Epi25 A1 Feng, Yen-Chen Anne A1 Howrigan, Daniel P A1 Abbott, Liam E A1 Tashman, Katherine A1 Cerrato, Felecia A1 Singh, Tarjinder A1 Heyne, Henrike A1 Byrnes, Andrea A1 Churchhouse, Claire A1 Watts, Nick A1 Solomonson, Matthew A1 Lal, Dennis A1 Heinzen, Erin L A1 Dhindsa, Ryan S A1 Stanley, Kate E A1 Cavalleri, Gianpiero L A1 Hakonarson, Hakon A1 Helbig, Ingo A1 Krause, Roland A1 May, Patrick A1 Weckhuysen, Sarah A1 Petrovski, Slavé A1 Kamalakaran, Sitharthan A1 Sisodiya, Sanjay M A1 Cossette, Patrick A1 Cotsapas, Chris A1 De Jonghe, Peter A1 Dixon-Salazar, Tracy A1 Guerrini, Renzo A1 Kwan, Patrick A1 Marson, Anthony G A1 Stewart, Randy A1 Depondt, Chantal A1 Dlugos, Dennis J A1 Scheffer, Ingrid E A1 Striano, Pasquale A1 Freyer, Catharine A1 McKenna, Kevin A1 Regan, Brigid M A1 Bellows, Susannah T A1 Leu, Costin A1 Bennett, Caitlin A A1 Johns, Esther MC A1 Macdonald, Alexandra A1 Shilling, Hannah A1 Burgess, Rosemary A1 Weckhuysen, Dorien A1 Bahlo, Melanie A1 O'Brien, Terence J A1 Todaro, Marian A1 Stamberger, Hannah A1 Andrade, Danielle M A1 Sadoway, Tara R A1 Mo, Kelly A1 Krestel, Heinz A1 Gallati, Sabina A1 Papacostas, Savvas S A1 Kousiappa, Ioanna A1 Tanteles, George A A1 Štěrbová, Katalin A1 Vlčková, Markéta A1 Sedláčková, Lucie A1 Laššuthová, Petra A1 Klein, Karl Martin A1 Rosenow, Felix A1 Reif, Philipp S A1 Knake, Susanne A1 Kunz, Wolfram S A1 Zsurka, Gábor A1 Elger, Christian E A1 Bauer, Jürgen A1 Rademacher, Michael A1 Pendziwiat, Manuela A1 Muhle, Hiltrud A1 Rademacher, Annika A1 van Baalen, Andreas A1 von Spiczak, Sarah A1 Stephani, Ulrich A1 Afawi, Zaid A1 Korczyn, Amos D A1 Kanaan, Moien A1 Canavati, Christina A1 Kurlemann, Gerhard A1 Müller-Schlüter, Karen A1 Kluger, Gerhard A1 Häusler, Martin A1 Blatt, Ilan A1 Lemke, Johannes R A1 Krey, Ilona A1 Weber, Yvonne G A1 Wolking, Stefan A1 Becker, Felicitas A1 Hengsbach, Christian A1 Rau, Sarah A1 Maisch, Ana F A1 Steinhoff, Bernhard J A1 Schulze-Bonhage, Andreas A1 Schubert-Bast, Susanne A1 Schreiber, Herbert PB eScholarship, University of California YR 2019 K1 Clinical Research K1 Human Genome K1 Neurosciences K1 Epilepsy K1 Biotechnology K1 Genetics K1 Neurodegenerative K1 Brain Disorders K1 2.1 Biological and endogenous factors K1 Aetiology K1 Neurological K1 Case-Control Studies K1 DNA Mutational Analysis K1 Exome K1 Genetic Markers K1 Genetic Predisposition to Disease K1 Genetic Variation K1 Humans K1 Phenotype K1 Exome Sequencing K1 Epi25 Collaborative. Electronic address: s.berkovic@unimelb.edu.au K1 Epi25 Collaborative K1 burden analysis K1 epileptic encephalopathy K1 seizures K1 sequencing K1 Biological Sciences K1 Medical and Health Sciences K1 Genetics & Heredity JF qt0wz3s560 LK http://dx.doi.org/https://escholarship.org/uc/item/0wz3s560 DO https://escholarship.org/uc/item/0wz3s560 SF ELIB - SuUB Bremen
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