A Shared Haplotype Indicates a Founder Event in Unverricht–Lundborg Disease Patients from Serbia-Reference-Cited by-同舟云学术

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A Shared Haplotype Indicates a Founder Event in Unverricht–Lundborg Disease Patients from Serbia

Published:2013-09-12 Issue:2 Volume:124 Page:102-109
ISSN:0020-7454
Container-title:International Journal of Neuroscience
language:en
Short-container-title:International Journal of Neuroscience

Author:

Kecmanović Miljana,Ristić Aleksandar J.,Ercegovac Marko,Keckarević-Marković Milica,Keckarević Dušan,Sokić Dragoslav,Romac Stanka

Publisher

Informa UK Limited

Subject

General Medicine,General Neuroscience

Link

http://www.tandfonline.com/doi/pdf/10.3109/00207454.2013.828723

Reference30 articles.

1. Clinical picture of EPM1-Unverricht-Lundborg disease

2. The Ramsay Hunt syndrome revisited: Mediterranean myoclonus versus mitochondrial encephalomyopathy with ragged-red fibers and Baltic myoclonus

3. Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutations

4. Clinical and Neurophysiological Development of Unverricht-Lundborg Disease in Four Swedish Siblings

Cited by 4 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. Genetic polymorphism of glutathione S-transferases: Relevance to neurological disorders;Pathophysiology;2018-12

2. First Molecular Diagnosis of a Patient with Unverricht-Lundborg Disease in Korea;Yonsei Medical Journal;2018

3. Role of Glutathione-S-transferases in neurological problems;Expert Opinion on Therapeutic Patents;2016-11-10

4. GSTA1, GSTM1, GSTP1 and GSTT1 polymorphisms in progressive myoclonus epilepsy: A Serbian case–control study;Seizure;2015-11

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