FAQ

CAPRIN1 is a gene that has been identified as playing a role in certain genetic conditions. Variants in this gene have been associated with neurodevelopmental and neurodegenerative disorders.

If you are a carrier of CAPRIN1, you may be eligible to participate in future studies.

If you meet the eligibility criteria below, simply complete the contact us form and connect with our research team for more information. Research into CAPRIN1 will help scientists better understand this mutation and find ways to improve diagnosis and treatments.

Eligibility criteria

· Confirmed genetic carrier of CAPRIN1.

· Willingness to provide genetic samples and participate in study interviews or surveys.

· Partake in discussions relating to potential trials and interventions including monitoring and observation of symptoms/traits.

If you meet these criteria, we encourage you to reach out and get involved!

CAPRIN1 Foundation focuses on raising awareness and understanding of this genetic mutation, particularly as it affects individual health and wellbeing.

CAPRIN1 Foundation is a global organisation, serving communities with resources and information on genetic mutations.

You can volunteer, participate in events or donate to support our mission of increasing awarenness of this life altering genetic mutation.

Yes, we offer a variety of educational materials to help individuals understand this genetic mutation and its implications.

We connect individuals with support networks and provide information to empower them in managing their genetic condition effectively.

Simply complete the participation form here and connect with our research team for more information.