Literature DB >> 33389126

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

Nevena Chakarova1, Lubomir Balabanski2,3, Rumyana Dimova4, Alexander Shinkov4, Tsvetalina Tankova4.   

Abstract

Entities:  

Keywords:  Berardinelli–Seip syndrome; Congenital generalized lipodystrophy; Lipoatrophic diabetes

Year:  2021        PMID: 33389126     DOI: 10.1007/s00592-020-01639-w

Source DB:  PubMed          Journal:  Acta Diabetol        ISSN: 0940-5429            Impact factor:   4.280


× No keyword cloud information.
  1 in total

Review 1.  Phenotypic and Genetic Characteristics of Lipodystrophy: Pathophysiology, Metabolic Abnormalities, and Comorbidities.

Authors:  Baris Akinci; Rasimcan Meral; Elif Arioglu Oral
Journal:  Curr Diab Rep       Date:  2018-11-08       Impact factor: 4.810

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.