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A novel heterozygous mutation in peroxisome proliferator-activated receptor-γ gene in a patient with familial partial lipodystrophy
Anil K. Agarwal
,
Abhimanyu Garg
Int Med - Nutrition & Met Dis
Internal Medicine
Research output
:
Contribution to journal
›
Article
›
peer-review
262
Scopus citations
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Dive into the research topics of 'A novel heterozygous mutation in peroxisome proliferator-activated receptor-γ gene in a patient with familial partial lipodystrophy'. Together they form a unique fingerprint.
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Medicine & Life Sciences
Familial Partial Lipodystrophy
100%
Peroxisome Proliferator-Activated Receptors
69%
Subcutaneous Fat
48%
Mutation
32%
Extremities
32%
Genes
23%
Diabetes Mellitus
22%
Lamin Type A
20%
Lipodystrophy
19%
Hirsutism
18%
Anthropometry
17%
Phenotype
17%
Hypertriglyceridemia
16%
Dyslipidemias
14%
Cysteine
13%
European Continental Ancestry Group
13%
Inborn Genetic Diseases
13%
Arginine
13%
Exons
12%
Insulin Resistance
11%
Nucleotides
11%
Magnetic Resonance Imaging
9%
Chemical Compounds
Mutation
48%
Fat
42%
Arginine Residue
17%
Insulin Derivative
14%
Cysteine
12%
Disorder
12%
White
12%
Nucleotide
11%
Resistance
9%