Autosomal recessive primary generalized dystonia in two siblings from a consanguineous family
Author:
Affiliation:
1. Department of Neurology, University of Michigan, Ann Arbor, Michigan, USA
2. Geriatric Research Education Clinical Center, Ann Arbor Veterans Affairs Medical Center, Ann Arbor, Michigan, USA
Funder
Veterans Affairs Merit Review
National Institutes of Health
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.20228
Reference16 articles.
1. Genetics of Primary Dystonia
2. The genetics of primary dystonias and related disorders
3. A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population
4. Four novel mutations in the Tyrosine Hydroxylase gene in patients with infantile parkinsonism
5. The genetics of idiopathic torsion dystonia.
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