After all, ALL LIVES ARE WORTH IT!
Keep up with the latest in research and knowledge about DEAF1.
We are an Institute for the promotion of research on DEAF1. Legally we are a non-profit association.
Our principles are transparency, ethics, the right to science, translation and dissemination of scientific knowledge, respect for life from its inception and socio-economic-environmental responsibility.
Vulto-Van Silfhout de Vries Syndrome are one of the conditions associated with the mutation in DEAF1 gene, with heterozygous genetical aspect. With subtitles in english, french and spanish.
Transparency is one of our founding principles.
Available in 4 languages (Portuguese, English, Spanish, French)
"Scientific progress must be illuminated with the light of faith, so that they respect the centrality of the human person."
Science is knowledge that comes from many, many experiences, studies, debates and collaborations. In this spirit, we join those who wish to deepen the knowledge of this gene, which is so important and essential for neurodevelopment and which has a direct impact on the Vulto-Van Silfhout de Vries Syndrome.
Do you want to follow up our studies? Do you want to participate in our raffles, charity events, campaigns? Want to help in some other way? Welcome!
Send us your contact. We will respond in a personalized way and we will always be available for direct dialogue.