Episodic ataxia in child with 16p11.2 deletion including PRRT2-Reference-Cited by-同舟云学术

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Episodic ataxia in child with 16p11.2 deletion including PRRT2

Published:2024-01 Issue: Volume:118 Page:105955
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Padmanabha Hansashree,Raghavendra K.,Arunachal Gautham,Nagaraj A.R.,Harishma R.S.,Nashi Saraswati,Pooja M.,Mathuranath P.S.,Mahale Rohan

Publisher

Elsevier BV

Subject

Neurology (clinical),Geriatrics and Gerontology,Neurology

Reference6 articles.

1. PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine;Gardiner;Neurology,2012

2. PRRT2-related phenotypes in patients with a 16p11.2 deletion;Vlaskamp;Eur. J. Med. Genet.,2019

3. The evolving spectrum of PRRT2-associated paroxysmal diseases;Ebrahimi-Fakhari;Brain,2015

5. Infantile convulsions and paroxysmal kinesigenic dyskinesia with 16p11.2 microdeletion;Dale;Neurology,2011

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Understanding copy number variations through their genes: a molecular view on 16p11.2 deletion and duplication syndromes;Frontiers in Pharmacology;2024-06-14

2. Rare Missense Variants in KCNJ10 Are Associated with Paroxysmal Kinesigenic Dyskinesia;Movement Disorders;2024-03-04

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