Disease | lipodystrophy |
Phenotype | C0221032|congenital lipodystrophy |
Sentences | 1 |
PubMedID- 21533227 | Here we report the analysis of a drosophila model of the most severe form of human lipodystrophy, berardinelli-seip congenital lipodystrophy 2, which is caused by mutations in the bscl2/seipin gene. |
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