Assessing the role ofDRD5 andDYT1 in two different case–control series with primary blepharospasm-Reference-Cited by-同舟云学术

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Assessing the role ofDRD5 andDYT1 in two different case–control series with primary blepharospasm

Published:2007 Issue:2 Volume:22 Page:162-166
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Clarimon Jordi,Brancati Francesco,Peckham Elizabeth,Valente Enza Maria,Dallapiccola Bruno,Abruzzese Giovanni,Girlanda Paolo,Defazio Giovanni,Berardelli Alfredo,Hallett Mark,Singleton Andrew B.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference17 articles.

1. A family study on primary blepharospasm

2. Familial blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene

3. The genetics of primary dystonias and related disorders

4. The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein

Cited by 46 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. Clinical implications of genetic polymorphisms in blepharospasm;Experimental and Therapeutic Medicine;2024-06-25

2. Blepharospasm and Hemifacial Spasm;Albert and Jakobiec's Principles and Practice of Ophthalmology;2022

3. Blepharospasm, Oromandibular Dystonia, and Meige Syndrome: Clinical and Genetic Update;Frontiers in Neurology;2021-03-29

4. Association of TOR1A and GCH1 Polymorphisms with Isolated Dystonia in India;Journal of Molecular Neuroscience;2020-07-13

5. Sex, blinking, and dry eye;Journal of Neurophysiology;2020-02-01

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