A novel biallelic LMNB2 variant in a patient with progressive myoclonus epilepsy and ataxia: A case of laminopathy

Abstract The report of LMNB2‐related progressive myoclonus epilepsy and ataxia due to missense homozygous c.473G>T variant.

Bibliographic Details
Main Authors:	Saeed Farajzadeh Valilou, Javad Karimzad Hagh, Mohammad Salimi Asl, Isa Abdi Rad, Masoud Edizadeh, Arash Pooladi
Format:	Article
Language:	English
Published:	Wiley 2021-08-01
Series:	Clinical Case Reports
Subjects:	ataxia laminopathy LMNB2 progressive myoclonus epilepsies whole‐exome sequencing
Online Access:	https://doi.org/10.1002/ccr3.4520

Internet

https://doi.org/10.1002/ccr3.4520