A familial t(4;8) translocation segregates with epilepsy and migraine with aura

A familial t(4;8) translocation segregates with epilepsy and migraine with aura

Abstract Three relatives carrying a t(4;8)(p15.2;p23.2) translocation had juvenile myoclonic epilepsy, self‐limited photosensitive occipital epilepsy and migraine with aura. The t(4;8) translocation interrupted the coding sequence of CSMD1 gene and occurred immediately to the 3’UTR of STIM2 gene. ST...

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Bibliographic Details
Main Authors: Milena Crippa, Paola Malatesta, Maria Teresa Bonati, Francesco Trapasso, Francesco Fortunato, Grazia Annesi, Lidia Larizza, Angelo Labate, Palma Finelli, Nicola Perrotti, Antonio Gambardella
Format: Article
Language:English
Published: Wiley 2020-05-01
Series:Annals of Clinical and Translational Neurology
Online Access:https://doi.org/10.1002/acn3.51040

Internet

https://doi.org/10.1002/acn3.51040

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