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

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

Author: Rauch, Anita; Wieczorek, Dagmar; Graf, Elisabeth; Wieland, Thomas; Endele, Sabine; Schwarzmayr, Thomas; Albrecht, Beate; Bartholdi, Deborah; Beygo, Jasmin; Di Donato, Nataliya; Dufke, Andreas; Cremer, Kirsten; Hempel, Maja; Horn, Denise; Hoyer, Juliane; Joset, Pascal; Ropke, Albrecht; Moog, Ute; Riess, Angelika; Thiel, Christian T.; Tzschach, Andreas; Wiesener, Antje; Wohlleber, Eva; Zweier, Christiane; Ekici, Arif B.; Zink, Alexander M.; Rump, Andreas; Meisinger, Christa; Grallert, Harald; Sticht, Heinrich; Schenck, Annette; Engels, Hartmut; Rappold, Gudrun; Schrock, Evelin; Wieacker, Peter; Riess, Olaf; Meitinger, Thomas; Reis, Andre; Strom, Tim M.
Tübinger Autor(en):
Dufke, Andreas
Tzschach, Andreas
Rieß, Olaf
Rieß, Angelika
Published in: Lancet (2012), Bd. 380, H. 9854, S. 1674-1682
Verlagsangabe: Elsevier Science Inc
Language: English
Full text: http://dx.doi.org/10.1016/S0140-6736(12)61480-9
ISSN: 0140-6736
DDC Classifikation: 610 - Medicine and health
Dokumentart: Artikel
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