We’re proud to support and attend the Cure CLCN4 Scientific Conference 2026, which brings together researchers, clinicians, families, and industry partners to accelerate progress in understanding and treating CLCN4-related neurodevelopmental conditions.

When: 18–19 June 2026
Venue: Friends House, 173–177 Euston Road, London NW1 2BJ

Visit the conference website for more information.

Meet Giovanna De Filippi to learn how our SSM-based electrophysiology platforms can support your CLC channel and transporter research, or to discuss your specific research questions, applications, and assay needs.

Learn more about CLCN4-related conditions.

About the Cure CLCN4 Scientific Conference

CLCN4-related neurodevelopmental condition (CLCN4-NDC) is a rare genetic disorder caused by mutations in the CLCN4 gene, which encodes the ClC-4 chloride/proton exchanger. The condition can lead to intellectual disability, epilepsy, movement disorders, and other neurological symptoms. Although much remains unknown about ClC-4 biology and disease mechanisms, the research community has grown rapidly in recent years. The conference brings together scientists, clinicians, and families to share new discoveries, discuss disease models and therapeutic approaches, and strengthen collaborations aimed at developing future treatments.