Frequently asked questions
What is CAPRIN1?
The CAPRIN1 gene (Cell Cycle Associated Protein 1) plays a key role in RNA processing, synaptic plasticity, and neurodevelopment. Variants in this gene have been associated with neurodevelopmental and neurodegenerative disorders.
Research into CAPRIN1 helps scientists better understand this mutation and find ways to improve diagnosis and treatments.
What is the main focus of CAPRIN1 Foundation?
CAPRIN1 Foundation focuses on raising awareness and understanding of this genetic mutation, particularly as it affects individual health and wellbeing.
Where is CAPRIN1 Foundation located?
CAPRIN1 Foundation is based in Greater London, England, United Kingdom, serving communities with resources and information on genetic mutations.
How can I get involved with CAPRIN1 Foundation?
You can volunteer, participate in events or donate to support our mission of increasing awarenness of this life altering genetic mutation.
Does CAPRIN1 Foundation provide educational resources?
Yes, we offer a variety of educational materials to help individuals understand this genetic mutation and its implications.
How does CAPRIN1 Foundation support affected individuals?
We connect individuals with support networks and provide information to empower them in managing their genetic condition effectively.
What do I need to do to participate?
Simply complete the participation form and connect with our research team for more information.