Indications of Linkage and Association of Gilles de la Tourette Syndrome in Two Independent Family Samples: 17q25 Is a Putative Susceptibility Region
- 1 October 2004
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 75 (4), 545-560
- https://doi.org/10.1086/424389
Abstract
No abstract availableKeywords
This publication has 81 references indexed in Scilit:
- Missense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human motoneuron diseaseThe Journal of cell biology, 2002
- A missense mutation in Tbce causes progressive motor neuronopathy in miceNature Genetics, 2002
- Mutation of TBCE causes hypoparathyroidism– retardation–dysmorphism and autosomal recessive Kenny–Caffey syndromeNature Genetics, 2002
- Basal ganglia dysfunction in Tourette’s syndrome: a new hypothesisPediatric Neurology, 2001
- Tubulin folding cofactor D is a microtubule destabilizing proteinFEBS Letters, 2000
- Complex segregation analysis of families ascertained through Gilles de la Tourette syndromeGenetic Epidemiology, 2000
- Genome scan for linkage to Gilles de la Tourette syndromeAmerican Journal of Medical Genetics, 1999
- Allelic discrimination using fluorogenic probes and the 5′ nuclease assayGenetic Analysis: Biomolecular Engineering, 1999
- Hypothesis: Homozygosity in tourette syndromeAmerican Journal of Medical Genetics, 1989
- The Inheritance of Gilles de la Tourette's Syndrome and Associated BehaviorsNew England Journal of Medicine, 1986