Association between the low molecular weight cytosolic acid phosphatase gene ACP1*A and comorbid features of Tourette syndrome.

Bottini, Nunzio; MacMurray, James; Rostamkani, Masoud; McGue, Matt; Iacono, William G; Comings, David E

Bottini, Nunzio; MacMurray, James; Rostamkani, Masoud; McGue, Matt; Iacono, William G; Comings, David E.

Affiliation

Bottini N; The Burnham Institute, La Jolla, CA, USA.

Neurosci Lett ; 330(2): 198-200, 2002 Sep 20.

Article in En | MEDLINE | ID: mdl-12231445

Subject(s)

Isoenzymes/genetics; Protein Tyrosine Phosphatases/genetics; Proto-Oncogene Proteins; Tourette Syndrome/genetics; Adolescent; Adult; Alleles; Attention Deficit Disorder with Hyperactivity/enzymology; Attention Deficit Disorder with Hyperactivity/epidemiology; Attention Deficit Disorder with Hyperactivity/genetics; Case-Control Studies; Child; Child, Preschool; Comorbidity; Cytosol/enzymology; Female; Gene Frequency; Genetic Variation; Genotype; Homozygote; Humans; Male; Middle Aged; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Tourette Syndrome/enzymology; Tourette Syndrome/epidemiology

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Database: MEDLINE Main subject: Tourette Syndrome / Proto-Oncogene Proteins / Protein Tyrosine Phosphatases / Isoenzymes Type of study: Observational_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Language: En Journal: Neurosci Lett Year: 2002 Type: Article Affiliation country: United States

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