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AAV liver gene therapy-mediated inhibition of FGF23 signaling as a therapeutic strategy for X-linked hypophosphatemia

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https://www.hal.inserm.fr/inserm-03413999
Contributor : Marie-Ange Di Carlo Connect in order to contact the contributor
Submitted on : Thursday, November 4, 2021 - 10:11:21 AM
Last modification on : Friday, January 21, 2022 - 3:34:18 AM

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Volha Zhukouskaya, Louisa Jauze, Séverine Charles, Christian Leborgne, Stéphane Hilliquin, et al.. AAV liver gene therapy-mediated inhibition of FGF23 signaling as a therapeutic strategy for X-linked hypophosphatemia. Endocrine Abstracts, Elsevier Science, 2021, ⟨10.1530/endoabs.73.OC6.2⟩. ⟨inserm-03413999⟩

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