Differences in circulating microRNA signature in Prader–Willi syndrome and non-syndromic obesity

Differences in circulating microRNA signature in Prader–Willi syndrome and non-syndromic obesity

Prader–Willi syndrome (PWS) represents the most common genetic-derived obesity disorder caused by the loss of expression of genes located on the paternal chromosome 15q11.2-q13. The PWS phenotype shows peculiar physical, endocrine and metabolic characteristics compared to those observed in non-syndr...

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Bibliographic Details
Main Authors: Devis Pascut, Sofia Tamini, Silvia Bresolin, Pablo Giraudi, Giuseppe Basso, Alessandro Minocci, Claudio Tiribelli, Graziano Grugni, Alessandro Sartorio
Format: Article
Language:English
Published: Bioscientifica 2018-11-01
Series:Endocrine Connections
Subjects:
microRNA
miRNA
Prader–Willi syndrome
array
obese
non-syndromic obesity
serum miRNA
Online Access:https://ec.bioscientifica.com/view/journals/ec/7/12/EC-18-0329.xml

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https://ec.bioscientifica.com/view/journals/ec/7/12/EC-18-0329.xml

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