Reply to: Comment on Soft cerebellar signs unveil <i>RARS2</i>‐related epilepsy-Reference-Cited by-同舟云学术

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Reply to: Comment on Soft cerebellar signs unveil RARS2‐related epilepsy

Published:2024-06-29 Issue: Volume: Page:
ISSN:1294-9361
Container-title:Epileptic Disorders
language:en
Short-container-title:Epileptic Disorders

Author:

Yahya Vidal¹^ORCID,Dilena Robertino²^ORCID,Monfrini Edoardo¹³

Affiliation:

1. Department of Pathophysiology and Transplantation, Dino Ferrari Center University of Milan Milan Italy

2. Neurophysiopathology Unit Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milan Italy

3. Neurology Unit Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milan Italy

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/epd2.20260

Reference3 articles.

1. DEPDC5 plays a vital role in epilepsy: Genotypic and phenotypic features in cohort and literature

2. Missense variants in ANO4 cause sporadic encephalopathic or familial epilepsy with evidence for a dominant-negative effect

3. Expanding the genetics and phenotypic spectrum of Lysine-specific demethylase 5C (KDM5C): a report of 13 novel variants

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