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Paving the way toward treatment solutions for CTNNB1 syndrome: a patient organization perspective

The CTNNB1 Connect & Cure and CTNNB1 Foundation, alongside Asociación CTNNB1, CTNNB1 Italia, Association CTNNB1 France, and researchers and clinicians globally are dedicated to finding effective treatments and cures for CTNNB1 syndrome. The syndrome is also characterized by progressive spasticity, w...

Whakaahuatanga katoa

I tiakina i:
Ngā kaituhi matua: Špela Miroševič, Shivang Khandelwal, Emily Amerson, Effie Parks, Mariana Parks, Lauren Cochran, Ana González Hernández, Mirela Ferraro, Leszek Lisowski, Andrea Perez-Iturralde, Wendy Chung, Michele H. Jacob, Nina Žakelj, Duško Lainšček, Vida Forstnerič, Petra Sušjan, Matea Maruna, Roman Jerala, Damjan Osredkar
Hōputu: Artigo
Reo:Inglês
I whakaputaina: SAGE Publishing 2025-02-01
Rangatū:Therapeutic Advances in Rare Disease
Urunga tuihono:https://doi.org/10.1177/26330040251318355
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