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

✍ Scribed by 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 Meisinger; Harald Grallert; Heinrich Sticht; Annette Schenck; Hartmut Engels; Gudrun Rappold; Evelin Schröck; Peter Wieacker; Olaf Riess; Thomas Meitinger; André Reis; Tim M Strom

• Book ID: 118185437
• Publisher: The Lancet
• Year: 2012
• Tongue: English
• Weight: 249 KB
• Volume: 380
• Category: Article
• ISSN: 0140-6736
• DOI: 10.1016/s0140-6736(12)61480-9