Welcome

This website provides information on patients with mutations in the DEAF1 gene, including clinical data, molecular data, management and research options.

This website was created to share and collect information about clinic, management and research projects to gather more knowledge and provide better treatment of patients with mutations in the DEAF1 gene.

Choose page:

• DEAF1 autosomal recessive
• DEAF1 autosomal dominant

Clinicals who identify a patient with a mutation in DEAF1 are invited to submit clinical and molecular information to the database.

Anneke Vulto-van Silfhout, MD,PhD, Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands, Anneke.Vulto-van Silfhout@radboudumc.nl

Lisenka Peart-Vissers, PhD, Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands, Lisenka.Vissers@radboudumc.nl

Bert de Vries, MD, PhD, Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands, Bert.deVries@radboudumc.nl

Maria J. Nabais Sá, MD,MPH,PhD, Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands, Maria.NabaisSa@radboudumc.nl

Philip J. Jensik, PhD, Department of Physiology, Southern Illinois University School of Medicine, Carbondale, IL 62901, USA, pjensik@siumed.edu