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International Journal of Neuroscience Volume 124, 2014 - Issue 2
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Research Article

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

Miljana KecmanovićFaculty of Biology, University of Belgrade, Belgrade, SerbiaCorrespondence[email protected]
,
Aleksandar J. RistićClinic of Neurology, Clinical Centre of Serbia, Medical Faculty, Belgrade, Serbia
,
Marko ErcegovacClinic of Neurology, Clinical Centre of Serbia, Medical Faculty, Belgrade, Serbia
,
Milica Keckarević-MarkovićFaculty of Biology, University of Belgrade, Belgrade, Serbia
,
Dušan KeckarevićFaculty of Biology, University of Belgrade, Belgrade, Serbia
,
Dragoslav SokićClinic of Neurology, Clinical Centre of Serbia, Medical Faculty, Belgrade, Serbia
&
Stanka RomacFaculty of Biology, University of Belgrade, Belgrade, Serbia
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Pages 102-109 | Received 01 Dec 2012, Accepted 22 Jul 2013, Published online: 12 Sep 2013

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Anil Kumar, Dinesh K. Dhull, Varun Gupta, Priyanka Channana, Arti Singh, Manveen Bhardwaj, Poonam Ruhal & Ruchika Mittal. (2017) Role of Glutathione-S-transferases in neurological problems. Expert Opinion on Therapeutic Patents 27:3, pages 299-309.
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Articles from other publishers (3)

Sreenivasulu Dasari, Sailaja Gonuguntla, Muni Swamy Ganjayi, Suman Bukke, Basha Sreenivasulu & Balaji Meriga. (2018) Genetic polymorphism of glutathione S-transferases: Relevance to neurological disorders. Pathophysiology 25:4, pages 285-292.
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Ki Hoon Kim, Ju Sun Song, Chan Wook ParkChang-Seok Ki & Kyoung Heo. (2018) First Molecular Diagnosis of a Patient with Unverricht-Lundborg Disease in Korea. Yonsei Medical Journal 59:6, pages 798.
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Marko Ercegovac, Nebojsa Jovic, Dragoslav Sokic, Ana Savic-Radojevic, Vesna Coric, Tanja Radic, Dimitrije Nikolic, Miljana Kecmanovic, Marija Matic, Tatjana Simic & Marija Pljesa-Ercegovac. (2015) GSTA1, GSTM1, GSTP1 and GSTT1 polymorphisms in progressive myoclonus epilepsy: A Serbian case–control study. Seizure 32, pages 30-36.
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