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2287 ECG and echo characteristics in familial partial lipodystrophy: The impact of Lamin A variants
OBJECTIVES/SPECIFIC AIMS: Familial partial lipodystrophy (FPLD) is an inherited, rare syndrome characterized by selective absence of adipose tissue from extremities which is associated with severe insulin resistance, and metabolic dyslipidemia (with hypertriglyceridemia, and low HDL) Typically, 30%–...
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| Pubblicato in: | J Clin Transl Sci |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Cambridge University Press
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6798885/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/cts.2018.164 |
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