Associated Papers
Biallelic novel CCDC186 loss-of-function variant disrupting the gene function causes neurodevelopmental phenotype and review of the literature.
Gezdirici A et al.
Brain & Development, 2025
Functional Evidence of CCDC186 as a New Disease-Associated Gene with Endocrine and Central Nervous System Alterations.
Arrabal L et al.
International Journal of Molecular Sciences, 2023
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