Abstract
With evidence from family, twin, and adoption studies, heredity appears to be a significant etiological factor in several neuropsychiatric disorders including schizophrenia (McGuffin 1988), bipolar affective disorder (Kidd and Weisman 1978), and Gilles de la Tourette’s syndrome (Pauls and Leckerman 1986). However, the mode of inheritance of these diseases is complex and does not follow simple mendelian expectations. In addition, the probable etiological heterogeneity of diseases such as schizophrenia complicates the analysis for linkage studies. Molecular biology has provided polymorphic DNA markers, which can be classified into two types. Nonspecific approaches utilize anonymous markers along the entire genome, the number of which strongly increases as the genome mapping becomes more detailed. This approach might be fruitful, but is a long and exacting task. On the other hand, if the underlying biological substrates for these diseases can be identified, then the gene(s) governing these substrates may constitute good candidate gene(s).
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Sokoloff, P., Lannfelt, L., Martres, M.P., Giros, B., Bouthenet, M.L., Schwartz, J.C. (1992). The D3 Dopamine Receptor Gene as a Candidate Gene for Genetic Linkage Studies. In: Mendlewicz, J., Hippius, H., Bondy, B., Ackenheil, M., Sandler, M. (eds) Genetic Research in Psychiatry. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-46762-2_10
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DOI: https://doi.org/10.1007/978-3-642-46762-2_10
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