Paper

Data

Name Rauch A, Wieczorek D, Graf E, Wieland T, Endele S, Schwarzmayr T, Albrecht B, Bartholdi D, Beygo J, Di Donato N, Dufke A, Cremer K, Hempel M, Horn D, Hoyer J, Joset P, Röpke A, Moog U, Riess A, Thiel CT, Tzschach A, Wiesener A, Wohlleber E, Zweier C, Ekici AB, Zink AM, Rump A, Meisinger C, Grallert H, Sticht H, Schenck A, Engels H, Rappold G, Schröck E, Wieacker P, Riess O, Meitinger T, Reis A, Strom TM (2012)

Description

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

References

Authors Rauch A Show Other Wieczorek D Show Other Graf E Show Other Wieland T Show Other Endele S Show Other Schwarzmayr T Show Other Albrecht B Show Other Bartholdi D Show Other Beygo J Show Other Di Donato N Show Other Dufke A Show Other Cremer K Show Other Hempel M Show Other Horn D Show Other Hoyer J Show Other Joset P Show Other Röpke A Show Other Moog U Show Other Riess A Show Other Thiel CT Show Other Tzschach A Show Other Wiesener A Show Other Wohlleber E Show Other Zweier C Show Other Ekici AB Show Other Zink AM Show Other Rump A Show Other Meisinger C Show Other Grallert H Show Other Sticht H Show Other Schenck A Show Other Engels H Show Other Rappold G Show Other Schröck E Show Other Wieacker P Show Other Riess O Show Other Meitinger T Show Other Reis A Show Other Strom TM Show Other

Volume 380

First page 1674

Last page 82

Publisher

Pubmed ID 23020937

Year published 2012

Month published

Day published

Journal or book name Lancet

Book Editor(s)

Missing References

Type

Digital Object Identifier 10.1016/S0140-6736(12)61480-9

URL

Stated Usage

Species