Mitochondrial Function in Gilles de la Tourette Syndrome Patients With and Without Intragenic IMMP2L Deletions

Author:

Bjerregaard Victoria A.,Schönewolf-Greulich Bitten,Juel Rasmussen Lene,Desler Claus,Tümer Zeynep

Funder

Lundbeckfonden

Publisher

Frontiers Media SA

Subject

Clinical Neurology,Neurology

Reference37 articles.

1. Gilles de la Tourette syndrome;Robertson;Nat Rev Dis Primers.,2017

2. Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3;Boghosian-Sell;Am J Hum Genet.,1996

3. Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome;Petek;Am J Hum Genet.,2001

4. Candidate region for Gilles de la Tourette syndrome at 7q31;Kroisel;Am J Med Genet.,2001

5. Association between 7q31 markers and Tourette syndrome;Díaz-Anzaldúa;Am J Med Genet A.,2004

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