Body Composition And Bone Mineral Differences According to Lamin A (LMNA) Genotype in Familial Partial Lipodystrophy Type 2

Phenotypic heterogeneity is well known in Familial Partial Lipodystrophy Type 2 (FPLD2), a rare form of adipose tissue disorder caused by pathogenic mutations in LMNA gene. Animal studies from our group have identified an association between adipose tissue loss and an increase in bone mineral densit...

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Bibliografische gegevens
Gepubliceerd in:J Endocr Soc
Hoofdauteurs: de Freitas, Maria Cristina Foss, Akinci, Baris, Corsa, Callie, Rothberg, Amy E, MacDougald, Ormond A, Oral, Elif A
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Oxford University Press 2021
Onderwerpen:
Bone and Mineral Metabolism
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC8089602/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvab048.550
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