Associated Papers
The genotype-phenotype correlations of the CACNA1A-related neurodevelopmental disorders: a small case series and literature reviews.
Kessi M et al.
Frontiers in Molecular Neuroscience, 2023
37555011 (PubMed )
Supplement: Table_2.docx
Clinical and molecular spectrum of P/Q type calcium channel Cav2.1 in epileptic patients.
Alehabib E et al.
Orphanet Journal of Rare Diseases, 2021
34727962 (PubMed )
Supplement: 13023_2021_2101_MOESM1_ESM.xlsx › supplementary_1
Calcium channelopathies and intellectual disability: a systematic review.
Kessi M et al.
Orphanet Journal of Rare Diseases, 2021
Diagnostic yield of targeted massively parallel sequencing in children with epileptic encephalopathy.
Kothur K et al.
Seizure, 2018
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