Last Updated: 09/26/2026
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Found 4 publications
Full-length isoform sequencing for resolving the molecular basis of Charcot-Marie-Tooth 2A.
Journal: bioRxiv : the preprint server for biology
Published: February 17, 2023
Full-length Isoform Sequencing for Resolving the Molecular Basis of Charcot-Marie-Tooth 2A.
Journal: Neurology. Genetics
Published: February 03, 2023
Dominant-negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome.
Journal: Annals of clinical and translational neurology
Published: January 30, 2023
New-onset Parkinsonism as a Covid-19 infection sequela: A systematic review and meta-analysis.
Journal: Annals of medicine and surgery (2012)
Published: May 31, 2022
Showing 1-4 of 4
Last Updated: 09/26/2026