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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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Bibliografski detalji
Izdano u:J Endocr Soc
Glavni autori: 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
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Online pristup: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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