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Slovenian family initiates research into rare genetic disease

Ljubljana, 13 April - The parents of Urban, a one-year-old boy who has been diagnosed with a rare neurodevelopmental disorder called the CTNNB1 syndrome, have initiated research to develop a therapy for treating the disorder. Now they are raising money to finance the team of scientists from around the world working on the project.

Logo of the CTNNB1 foundation raiisng money for development of a medicine for a rare neurodevelopmental disorder.
Photo: The CTNNB1 foundation

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