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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Bibliografske podrobnosti
izdano v:J Endocr Soc
Main Authors: de Freitas, Maria Cristina Foss, Akinci, Baris, Corsa, Callie, Rothberg, Amy E, MacDougald, Ormond A, Oral, Elif A
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2021
Teme:
Bone and Mineral Metabolism
Online dostop: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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