학술논문
Exome sequencing revealed a p.G299R mutation in the COMP gene in an Iranian family suffering from pseudoachondroplasia.
Document Type
Article
Author
Source
Journal of Gene Medicine; Aug2019, Vol. 21 Issue 8, pN.PAG-N.PAG, 1p
Subject
Language
ISSN
1099498X
Abstract
Copyright of Journal of Gene Medicine is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)