- Record: found
- Abstract: found
- Article: not found
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Anita Rauch
1 ,
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 Meisinger ,
Harald Grallert ,
Heinrich Sticht ,
Annette Schenck ,
Hartmut Engels ,
Gudrun Rappold ,
Evelin Schröck ,
Peter Wieacker ,
Olaf Riess ,
Thomas Meitinger ,
André Reis ,
Tim M Strom
Nov 10 2012
There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.
Abstract
The genetic cause of intellectual disability in most patients is unclear because of the absence of morphological clues, information about the position of such genes, and suitable screening methods. Our aim was to identify de-novo variants in individuals with sporadic non-syndromic intellectual disability.