CSNK2A1 Foundation

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CSNK2A1 Foundation is focused on finding a cure for Okur-Chung Neurodevelopmental Syndrome and ensuring affected individuals have the opportunities and supports necessary for happy and full lives. CSNK2A1 Foundation is operated and funded through a committed team of volunteers, advocates and researchers. We aim to accomplish our mission by: * financing and encouraging meaningful research, * providing support to individuals affected and those that care for and love them, * promoting awareness, * educating patients, caregivers and health professionals and * advocating for issues important to our community. Okur-Chung Neurodevelopmental Syndrome is a rare genetic disorder first identified in 2016. OCNDS is caused by a mutation in the CSNK2A1 gene which is located on Chromosome 20. The gene CSNK2A1 creates a protein called CK2 which plays a crucial role in development. A mutation in this gene disrupts typical development. CSNK2A1 Foundation is a 501(c)(3) non-profit organization. EIN #82-4220939

Company Details

Employees
11
Founded
-
Address
1929 Van Ness Ave, San Francisco,california,united States
Industry
Philanthropic Fundraising Services
Website
http://www.csnk2a1foundation.org
Keywords
San Francisco.
HQ
San Francisco, California
Competitors
Orchard Lake Group, Probably Genetic, Allen Institute, TSC Alliance, National Organization for Rare Disorders, Tatton Brown Rahman Syndrome (TBRS) Community Inc., YWHAG Research Foundation, OlaWell, PACS1 Syndrome Research Foundation, CACNA1A Foundation.
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