Associated Papers
Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic features.
Soares RMV et al.
Frontiers in Endocrinology, 2024
Genetics and Clinical Characteristics of PPARγ Variant-Induced Diabetes in a Chinese Han Population.
Gong S et al.
Frontiers in Endocrinology, 2021
Natural helix 9 mutants of PPARγ differently affect its transcriptional activity.
Broekema MF et al.
Molecular Metabolism, 2019
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