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Clinical and molecular genetics of primary dystonias.

Abstract:

Primary dystonias are movement disorders with dystonia as a major symptom. They are frequently inherited as Mendelian traits. There are at least eight clinically distinct autosomal dominant and two X-linked recessive forms. In addition, pedigree analyses suggest the occurrence of an autosomal recessive variant. The clinical classification is increasingly being replaced by a genetic one. To date gene loci have been identified in at least six autosomal dominant forms, i.e., in idiopathic torsio...

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Publication status:
Published

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Publisher copy:
10.1007/s100480050025

Authors


Müller, U More by this author
Steinberger, D More by this author
Németh, AH More by this author
Journal:
Neurogenetics
Volume:
1
Issue:
3
Pages:
165-177
Publication date:
1998-03-05
DOI:
EISSN:
1364-6753
ISSN:
1364-6745
URN:
uuid:1a033a54-62c2-4b76-8c41-785ffc9bb623
Source identifiers:
438077
Local pid:
pubs:438077

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