Associated Papers
Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies.
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European Journal of Human Genetics : Ejhg, 2022
35017693 (PubMed )
Supplement: 41431_2021_1027_MOESM5_ESM.xlsx › Tabelle1
Congenital Mirror Movements Associated With Brain Malformations.
Nissenkorn A et al.
Journal of Child Neurology, 2021
Utility of Whole Exome Sequencing for Genetic Diagnosis of Previously Undiagnosed Pediatric Neurology Patients.
Kuperberg M et al.
Journal of Child Neurology, 2016
27572814 (PubMed )
Supplement: kuperberg_supp.pdf
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