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Author Report for: Capel E

No contact information in database for Capel E

    Title: EPHX1 mutations cause a lipoatrophic diabetes syndrome due to impaired epoxide hydrolysis and increased cellular senescence
    Gautheron J, Morisseau C, Chung WK, Zammouri J, Auclair M, Baujat G, Capel E, Moulin C, Wang Y and Jeru I <7 more author(s)>
    Ref: Elife, 10:, 2021 : PubMed


    Title: LIPE-related lipodystrophic syndrome: clinical characteristics and disease modelling using adipose stem cells
    Sollier C, Capel E, Aguilhon C, Smirnov V, Auclair M, Douillard C, Ladsous M, Defoort-Dhellemmes S, Gorwood J and Jeru I <6 more author(s)>
    Ref: European Journal of Endocrinology, 184:155, 2021 : PubMed


    Title: Lipodystrophic syndromes: From diagnosis to treatment
    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 : PubMed


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