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CTNNB1 Gene Mutation

Clinical trial condition

CTNNB1 Gene Mutation

Explore clinical trials studying CTNNB1 Gene Mutation. Study availability and eligibility vary by location and protocol.

3 public trials 1 recruiting study

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CTNNB1 Gene Mutation trial results

Recruiting

Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight

NCT01238250

Conditions: 15Q13.3 Deletion Syndrome, 15Q24 Deletion, 15q11.2 BP1-BP2 Deletion, +211 more
Locations: Boston Children's Hospital Boston, Massachusetts, United States

Geisinger Health System Lewisburg, Pennsylvania, United States

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Completed

Hyperekplexia in Patients With CTNNB1 Mutation

NCT05168969

Conditions: CTNNB1 Gene Mutation, Central Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
Locations: Chu Saint-Etienne Saint-Etienne, France

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Completed

Genotype-phenotype Correlations in Children and Adults With CTNNB1 Mutation

NCT04812119

Conditions: Autism Spectrum Disorder, CTNNB1 Gene Mutation, Child Development Disorders, Pervasive, +9 more
Locations: The University of Sydney Sydney, Australia

Children's Medical Research Institute Westmead, Australia

University Medical Centre Ljubljana Ljubljana, Slovenia

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