Familial blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene-Reference-Cited by-同舟云学术

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

Published:2003-01-21 Issue:2 Volume:18 Page:207-212
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Defazio Giovanni,Brancati Francesco,Valente Enza Maria,Caputo Viviana,Pizzuti Antonio,Martino Davide,Abbruzzese Giovanni,Livrea Paolo,Berardelli Alfredo,Dallapiccola Bruno

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference23 articles.

1. Tolcapone: COMT inhibition for the treatment of Parkinson's disease

2. Blepharospasm: a review of 264 patients.

3. A genetic study of idiopathic focal dystonias

4. Genetic Contribution to Idiopathic Adult-Onset Blepharospasm and Cranial-Cervical Dystonia

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