Genotype–phenotype correlations in THAP1 dystonia: Molecular foundations and description of new cases

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منابع مشابه

THAP1 Mutations and Dystonia Phenotypes: Genotype Phenotype Correlations

THAP1 mutations have been shown to be the cause of DYT6. A number of different mutation types and locations in the THAP1 gene have been associated with a range of severity and dystonia phenotypes, but, as yet, it has been difficult to identify clear genotype phenotype patterns. Here, we screened the THAP1 gene in a further series of dystonia cases and evaluated the mutation pathogenicity in thi...

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Mutations in THAP1/DYT6 reveal that diverse dystonia genes disrupt similar neuronal pathways and functions

Dystonia is characterized by involuntary muscle contractions. Its many forms are genetically, phenotypically and etiologically diverse and it is unknown whether their pathogenesis converges on shared pathways. Mutations in THAP1 [THAP (Thanatos-associated protein) domain containing, apoptosis associated protein 1], a ubiquitously expressed transcription factor with DNA binding and protein-inter...

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Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study.

BACKGROUND Mutations in THAP1 were recently identified as the cause of DYT6 primary dystonia; a founder mutation was detected in Amish-Mennonite families, and a different mutation was identified in another family of European descent. To assess more broadly the role of this gene, we screened for mutations in families that included one family member who had early-onset, non-focal primary dystonia...

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ژورنال

عنوان ژورنال: Parkinsonism & Related Disorders

سال: 2012

ISSN: 1353-8020

DOI: 10.1016/j.parkreldis.2012.02.001