|
ARCN1 Mutations Cause a Recognizable Craniofacial Syndrome Due to COPI-Mediated Transport Defects |
|
|
|
Title: |
ARCN1 Mutations Cause a Recognizable Craniofacial Syndrome Due to COPI-Mediated Transport Defects |
Author: |
Izumi, Kosuke Brett, Maggie Nishi, Eriko Drunat, Séverine Tan, Ee-Shien Fujiki, Katsunori Lebon, Sophie Cham, Breana Masuda, Koji Arakawa, Michiko Jacquinet, Adeline Yamazumi, Yusuke Chen, Shu-Ting Verloes, Alain Okada, Yuki Katou, Yuki Nakamura, Tomohiko Akiyama, Tetsu Gressens, Pierre Foo, Roger Passemard, Sandrine Tan, Ene-Choo El Ghouzzi, Vincent Shirahige, Katsuhiko |
Appeared in: |
The American journal of human genetics |
Paging: |
Volume 99 (2016) nr. 2 pages 9 p. |
Year: |
2016 |
Contents: |
|
Publisher: |
American Society of Human Genetics |
Source file: |
Elektronische Wetenschappelijke Tijdschriften |
|
|
|
|