Functional genomics in Drosophila models of human disease
It is occasionally observed that common sporadic diseases have rare familial counterparts in which mutations at a single locus result in a similar disorder exhibiting simple Mendelian inheritance. Such an observation is often sufficient justification for the creation of a disease model in the fly. W...
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Veröffentlicht in: | Briefings in functional genomics 2012-09, Vol.11 (5), p.405-415 |
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Format: | Artikel |
Sprache: | eng |
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