Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

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Author:Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato, Andreas Dufke, Kirsten Cremer, Maja Hempel, Denise Horn, Juliane Hoyer, Pascal Joset, Albrecht Röpke, Ute Moog, Angelika Riess, Christian T Thiel, Andreas Tzschach, Antje Wiesener, Eva Wohlleber, Christiane Zweier, Arif B Ekici, Alexander M Zink, Andreas Rump, Christa MeisingerGND, Harald Grallert, Heinrich Sticht, Annette Schenck, Hartmut Engels, Gudrun Rappold, Evelin Schröck, Peter Wieacker, Olaf Riess, Thomas Meitinger, André Reis, Tim M Strom
Frontdoor URLhttps://opus.bibliothek.uni-augsburg.de/opus4/85434
ISSN:0140-6736OPAC
Parent Title (English):The Lancet
Publisher:Elsevier BV
Type:Article
Language:English
Year of first Publication:2012
Release Date:2021/04/16
Volume:380
Issue:9854
First Page:1674
Last Page:1682
DOI:https://doi.org/10.1016/s0140-6736(12)61480-9
Institutes:Medizinische Fakultät
Medizinische Fakultät / Universitätsklinikum
Medizinische Fakultät / Lehrstuhl für Epidemiologie