학술논문
CCDC22: a novel candidate gene for syndromic X-linked intellectual disability.
Document Type
Letter
Author
Source
Subject
*LETTERS to the editor
*X chromosome abnormalities
*
Language
ISSN
1359-4184
Abstract
A letter to the editor is presented on CCDC22 as a new X-linked intellectual disability (XLID) candidate gene for targeted sequencing studies.