Progress in the search for genetic linkage with Tourette syndrome: An exclusion map covering more than 50% of the autosomal genome

Gilles de la Tourette syndrome is a neuropsychiatric disorder with an autosomal dominant mode of inheritance and reduced penetrance at a single genetic locus. Several research groups have genetic linkage studies underway to detect the chromosomal location of the gene that predisposes for this disord...

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Bibliographische Detailangaben
Hauptverfasser: Pakstis, Andrew J., Heutink, Peter, Pauls, David L., Kurlan, Roger, van de Wetering, Ben J. M., Leckman, James F., Sandkuyl, Lodewijk A., Kidd, Judith R., Breedveld, Guido J., Castiglione, Carmela M., Weber, James, Sparkes, Robert S., Cohen, Donald J., Kidd, Kenneth K., Oostra, Ben A.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 1991
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Original Articles
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683024/
https://ncbi.nlm.nih.gov/pubmed/1990837
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