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Single base deletion in the vasopressin gene is the cause of diabetes insipidus in Brattleboro rats Hartwig Schmale & Dietmar Richter
Abteilung Zellbiochemie, Institut für Physiologische Chemie, Universität Hamburg, Martinistrasse 52, D-2000 Hamburg 20, FRG
In rats with hereditary hypothalamic diabetes insipidus (Brattleboro rats) the gene for the vasopressin precursor lacks a single G residue in the protein-coding region. The mutation gives rise to an open reading frame predicting a hormone precursor having a different C-terminus.
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