APA (7th ed.) Citation

D, L., K, R., KM, S., P, H., N, C., D, B., . . . B, V. (2026). FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss. MedRxiv : the preprint server for health sciences. https://doi.org/10.64898/2026.03.27.26349271

Chicago Style (17th ed.) Citation

D, Liedtke, et al. "FRMPD4, a Causal Gene for Intellectual Disability and Epilepsy, Is Associated with X-linked Non-syndromic Hearing Loss." MedRxiv : The Preprint Server for Health Sciences 2026. https://doi.org/10.64898/2026.03.27.26349271.

MLA (9th ed.) Citation

D, Liedtke, et al. "FRMPD4, a Causal Gene for Intellectual Disability and Epilepsy, Is Associated with X-linked Non-syndromic Hearing Loss." MedRxiv : The Preprint Server for Health Sciences, 2026, https://doi.org/10.64898/2026.03.27.26349271.

Warning: These citations may not always be 100% accurate.