Associated Papers
Microtubule-Associated Serine/Threonine (MAST) Kinases in Development and Disease.
Rumpf M et al.
International Journal of Molecular Sciences, 2023
MAST1 variant causes mega-corpus-callosum syndrome with cortical malformations but without cerebellar hypoplasia.
Rodríguez-García ME et al.
American Journal of Medical Genetics. Part A, 2020
Evaluating the Role of MAST1 as an Intellectual Disability Disease Gene: Identification of a Novel De Novo Variant in a Patient with Developmental Disabilities.
Ben-Mahmoud A et al.
Journal of Molecular Neuroscience : Mn, 2020
Prioritized High-Confidence Risk Genes for Intellectual Disability Reveal Molecular Convergence During Brain Development.
Liu Z et al.
Frontiers in Genetics, 2018
30279698 (PubMed )
Supplement: Table_2.XLS › Sheet1
Genome sequencing identifies major causes of severe intellectual disability.
Gilissen C et al.
Nature, 2014
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