Associated Papers
MAP1B Variants Disrupt Neuronal Migration: Insights From Three Novel Families.
Archer J et al.
Clinical Genetics, 2026
Bilateral frontal periventricular nodular heterotopia: a distinctive cortical malformation.
Hoogwijs I et al.
European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society, 2025
Novel MAP1B loss-of-function variant associated with periventricular nodular heterotopia 9 and literature review on genotype-phenotype associations of MAP1B.
Zhou C et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2025
MAP1B related syndrome: Case presentation and review of literature.
Julca DM et al.
American Journal of Medical Genetics. Part A, 2019
MAP1B mutations cause intellectual disability and extensive white matter deficit.
Walters GB et al.
Nature Communications, 2018
De novo and inherited private variants in MAP1B in periventricular nodular heterotopia.
Heinzen EL et al.
Plos Genetics, 2018
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