Associated Papers
Atypical GNAO1 variants in severe childhood speech disorders: clinical, genetic, and molecular insights.
Larasati YA et al.
Molecular Autism, 2025
Clinical-molecular profiling of atypical GNAO1 patients: Novel pathogenic variants, unusual manifestations, and severe molecular dysfunction.
Solis GP et al.
Genes & Diseases, 2025
Dominant Gα mutations in human disease: unifying mechanisms and treatment strategies.
Katanaev VL et al.
Embo Molecular Medicine, 2025
40745211 (PubMed )
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