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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Bibliografiset tiedot
Julkaisussa:J Endocr Soc
Päätekijät: de Freitas, Maria Cristina Foss, Akinci, Baris, Corsa, Callie, Rothberg, Amy E, MacDougald, Ormond A, Oral, Elif A
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2021
Aiheet:
Bone and Mineral Metabolism
Linkit: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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