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A novel AGPAT2 mutation associated with a case of late-diagnosed congenital generalized lipodystrophy type 1

Nevena Chakarova1, Lubomir Balabanski2,3, Rumyana Dimova4

  • 1Department of Endocrinology, Medical University of Sofia, 2 Zdrave Str, 1431, Sofia, Bulgaria. veni_chakarova@abv.bg.

Acta Diabetologica
|January 3, 2021
PubMed
Abstract

No abstract available in PubMed .

Keywords:
Berardinelli–Seip syndromeCongenital generalized lipodystrophyLipoatrophic diabetes

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