Associated Papers
The Role of a Novel TRIP12 Mutation in Intellectual Disability: A Molecular and Clinical Investigation in Multiplex Family.
Nobakht R et al.
Journal of Molecular Neuroscience : Mn, 2025
The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant.
Aerden M et al.
European Journal of Human Genetics : Ejhg, 2023
Episignature Mapping of TRIP12 Provides Functional Insight into Clark-Baraitser Syndrome.
van der Laan L et al.
International Journal of Molecular Sciences, 2022
Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features.
Zhang J et al.
Human Genetics, 2017
Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features.
Zhang J et al.
Human Genetics, 2017
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