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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Huntington's disease in two New Britain families
Abstract:
In East New Britain, Papua New Guinea, two Melanesian families were studied in which the typical features of Hungtington's disease were observed in clinically affected members. Mendelian autosomal dominant inheritance was indicated by the respective family trees.
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