Associated Papers
Heterozygous truncating variant of TAOK1 in a boy with periventricular nodular heterotopia: a case report and literature review of TAOK1-related neurodevelopmental disorders.
Cavalli A et al.
Bmc Medical Genomics, 2024
38443934 (PubMed )
Supplement: 12920_2024_1840_MOESM1_ESM.xlsx › Foglio1
Paternal De Novo Variant of TAOK1 in a Fetus With Structural Brain Abnormalities.
Yu L et al.
Frontiers in Genetics, 2022
Clinical and Neurobiological Aspects of TAO Kinase Family in Neurodevelopmental Disorders.
Hu C et al.
Frontiers in Molecular Neuroscience, 2021
De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders.
Dulovic-Mahlow M et al.
American Journal of Human Genetics, 2019
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