Feve B

References (2)

Title : EPHX1 mutations cause a lipoatrophic diabetes syndrome due to impaired epoxide hydrolysis and increased cellular senescence - Gautheron_2021_Elife_10_
Author(s) : Gautheron J , Morisseau C , Chung WK , Zammouri J , Auclair M , Baujat G , Capel E , Moulin C , Wang Y , Yang J , Hammock BD , Cerame B , Phan F , Feve B , Vigouroux C , Andreelli F , Jeru I
Ref : Elife , 10 : , 2021
PubMedID: 34342583
Gene_locus related to this paper: human-EPHX1

Title : Lipodystrophic syndromes: From diagnosis to treatment - Sollier_2020_Ann.Endocrinol.(Paris)_81_51
Author(s) : Sollier C , Vatier C , Capel E , Lascols O , Auclair M , Janmaat S , Feve B , Jeru I , Vigouroux C
Ref : Ann Endocrinol (Paris) , 81 :51 , 2020
PubMedID: 31982105