Whole-exome sequencing identifies ADRA2A mutation in atypical familial partial lipodystrophy-Reference-Cited by-同舟云学术

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Whole-exome sequencing identifies ADRA2A mutation in atypical familial partial lipodystrophy

Published:2016-06-16 Issue:9 Volume:1 Page:
ISSN:2379-3708
Container-title:JCI Insight
language:en
Short-container-title:

Author:

Garg Abhimanyu,Sankella Shireesha,Xing Chao,Agarwal Anil K.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference41 articles.

1. Acquired and Inherited Lipodystrophies

2. Lipodystrophies: Genetic and Acquired Body Fat Disorders

3. The genetics of lipid storage and human lipodystrophies

4. Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy

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1. Lipodystrophic Laminopathies: From Dunnigan Disease to Progeroid Syndromes;International Journal of Molecular Sciences;2024-08-28

2. G protein-coupled receptor (GPCR) pharmacogenomics;Critical Reviews in Clinical Laboratory Sciences;2024-08-09

3. Roles of lipid droplets and related proteins in metabolic diseases;Lipids in Health and Disease;2024-07-19

4. Serum levels of adiponectin differentiate generalized lipodystrophies from anorexia nervosa;Journal of Endocrinological Investigation;2024-02-15

5. Body Fat Distribution Contributes to Defining the Relationship between Insulin Resistance and Obesity in Human Diseases;Current Diabetes Reviews;2023-08-16

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