Using the clinical picture of triplet repeat disorders as a
starting point, this work reviews and integrates understanding of
the molecular pathologies, the genotype-phenotype relationships,
and the mutational processes of trinucleotide repeats of triplet
repeat disorders. Laboratory and clinical issues relating to
genetic testing for these disorders are also addressed. This book
is aimed at clinicians and researchers in genetics, neuroscience,
paediatrics and psychiatry.
General
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