Clinical and Molecular Characterization of a Severe Form of Partial Lipodystrophy Expanding the Phenotype of PPARγ Deficiency

Journal of Lipid Research - United States
doi 10.1194/jlr.p025437
Full Text
Abstract

Available in full text

Date
Authors
Publisher

American Society for Biochemistry & Molecular Biology (ASBMB)

Related search

PNPO Deficiency and Cirrhosis: Expanding the Clinical Phenotype?

JIMD Reports
Internal MedicineGeneticsMolecular BiologyBiochemistryEndocrinologyMetabolismDiabetes
2015English

Expanding the Clinical Phenotype of the 3q29 Microdeletion Syndrome and Characterization of the Reciprocal Microduplication

Molecular Cytogenetics
BiochemistryMolecular MedicineGeneticsMolecular Biology
2008English

Acquired Partial Lipodystrophy

2020English

Association of Partial Lipodystrophy and Sjögren's Syndrome

Japanese Journal of Clinical Immunology
1983English

Expanding the Phenotype Half of the Genotype−phenotype Space

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2016English

Clinical and Molecular Heterogeneity of RTEL1 Deficiency

Frontiers in Immunology
AllergyImmunology
2017English

Mutations inRIT1cause Noonan Syndrome - Additional Functional Evidence and Expanding the Clinical Phenotype

Clinical Genetics
Genetics
2015English

Is Severe Obesity a Form of Addiction?: Rationale, Clinical Approach, and Controlled Clinical Trial

CyberPsychology & Behavior
2006English

LIPE-related Familial Partial Lipodystrophy

2020English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy