Scroll
To Top
0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

*Important

The information contained in the Organizational Database (ODB) is provided for informational purposes only. There is no implied endorsement by NORD. NORD does not promote or endorse participation in any specific organization. The information is subject to change without notice. Every effort is made to ensure that the details for each entry are as current as possible.


CAMK2 Therapeutics Network


Email Address

[email protected]

Description

CAMK2 Therapeutics Network is a family-led, scientifically supported international collaboration working to improve the lives of individuals with CAMK2 genetic mutations. The rare gene mutations result in severe neurodevelopmental disorders that affect our loved ones and pose extreme challenges for family life. We aim to nurture a strong CAMK2 community and, in partnership with our medical and scientific colleagues, to work toward developing near-term treatments by repurposing medications. Our long-term goal is to use precision genetics to develop a cure. Facebook: https://www.facebook.com/CAMK2TherapeuticsNetwork

Please Note

The National Organization for Rare Disorders (NORD) web site, its databases, and the contents thereof are copyrighted by NORD. No part of the NORD web site, databases, or the contents may be copied in any way, including but not limited to the following: electronically downloading, storing in a retrieval system, or redistributing for any commercial purposes without the express written permission of NORD. Permission is hereby granted to print one hard copy of the information on an individual disease for your personal use, provided that such content is in no way modified, and the credit for the source (NORD) and NORD’s copyright notice are included on the printed copy. Any other electronic reproduction or other printed versions is strictly prohibited.

NORD's Rare Disease Information Database is copyrighted and may not be published without the written consent of NORD.