Ontology highlight
ABSTRACT:
SUBMITTER: Mancina RM
PROVIDER: S-EPMC8803605 | biostudies-literature | 2022 Jan
REPOSITORIES: biostudies-literature
Mancina Rosellina M RM Sasidharan Kavitha K Lindblom Anna A Wei Ying Y Ciociola Ester E Jamialahmadi Oveis O Pingitore Piero P Andréasson Anne-Christine AC Pellegrini Giovanni G Baselli Guido G Männistö Ville V Pihlajamäki Jussi J Kärjä Vesa V Grimaudo Stefania S Marini Ilaria I Maggioni Marco M Becattini Barbara B Tavaglione Federica F Dix Carly C Castaldo Marie M Klein Stephanie S Perelis Mark M Pattou Francois F Thuillier Dorothée D Raverdy Violeta V Dongiovanni Paola P Fracanzani Anna Ludovica AL Stickel Felix F Hampe Jochen J Buch Stephan S Luukkonen Panu K PK Prati Daniele D Yki-Järvinen Hannele H Petta Salvatore S Xing Chao C Schafmayer Clemens C Aigner Elmar E Datz Christian C Lee Richard G RG Valenti Luca L Lindén Daniel D Romeo Stefano S
Nature metabolism 20220131 1
Fatty liver disease (FLD) is a growing health issue with burdening unmet clinical needs. FLD has a genetic component but, despite the common variants already identified, there is still a missing heritability component. Using a candidate gene approach, we identify a locus (rs71519934) at the Pleckstrin and Sec7 domain-containing 3 (PSD3) gene resulting in a leucine to threonine substitution at position 186 of the protein (L186T) that reduces susceptibility to the entire spectrum of FLD in individ ...[more]