Haplotype‐controlled analysis of the association of a non‐synonymous single nucleotide polymorphism at DBH (+ 1603C → T) with plasma dopamine β‐hydroxylase activity-Reference-Cited by-同舟云学术

Haplotype‐controlled analysis of the association of a non‐synonymous single nucleotide polymorphism at DBH (+ 1603C → T) with plasma dopamine β‐hydroxylase activity

Published:2005-09-08 Issue:1 Volume:139B Page:88-90
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Tang Yilang¹,Anderson George M.²,Zabetian Cyrus P.³,Köhnke Michael D.⁴,Cubells Joseph F.¹

Affiliation:

1. Department of Psychiatry, Yale University School of Medicine and VA Connecticut Healthcare System, West Haven, Connecticut

2. Yale Child Study Center, Yale University School of Medicine, New Haven, Connecticut

3. Department of Neurology, University of Washington School of Medicine and Geriatric Research Education and Clinical Center, VA Puget Sound Health Care System, Seattle, Washington

4. University Hospital of Psychiatry and Psychotherapy, Tübingen University Hospital, Tübingen, Germany

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.b.30220

Reference15 articles.

1. Human genetics of plasma dopamine ?-hydroxylase activity: applications to research in psychiatry and neurology

2. Population genetics of a functional variant of the dopamine β-hydroxylase gene (DBH)

3. Dopamine β-hydroxylase: two polymorphisms in linkage disequilibrium at the structural gene DBH associate with biochemical phenotypic variation

4. Genotype-controlled analysis of plasma dopamine β-hydroxylase activity in psychotic unipolar major depression

5. Human serum dopamine beta‐hydroxylase: Correlation of enzymatic activity with immunoreactive protein in genetically defined samples;Dunnette J;Am J Hum Genet,1976

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