Exclusion of linkage between manic depressive illness and tyrosine hydroxylase and dopamine D2 receptor genes

Psychiatr Genet. 1994 Spring;4(1):13-22. doi: 10.1097/00041444-199421000-00003.

Abstract

Mutations at the tyrosine hydroxylase or dopamine D2 receptor loci causing manic depressive illness are unlikely in two families reported here. Linkage was excluded for both loci assuming a dominant mode of transmission and for the tyrosine hydroxylase locus also assuming a recessive mode of transmission. The exclusion was significant using models based on severity of psychopathology and a model requiring severe illness also in first-degree relatives. Conservative genetic parameters were used to minimize misclassification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Base Sequence
  • Bipolar Disorder / genetics*
  • Female
  • Genetic Linkage*
  • Genetic Markers
  • Humans
  • Lod Score
  • Male
  • Molecular Sequence Data
  • Pedigree
  • Receptors, Dopamine D2 / genetics*
  • Tyrosine 3-Monooxygenase / genetics*

Substances

  • Genetic Markers
  • Receptors, Dopamine D2
  • Tyrosine 3-Monooxygenase