Agnes Linglart, MD, PHD

INSERM U986, Service d'Endocrinologie Pédiatrique, Hôpital Bicêtre
Université Paris Sud – Centre de référence des maladies rares du métabolisme du calcium et du phosphore
Papers:
Functional characterization of PRKAR1A mutants causing acrodysostosis with hormonal resistance
Anticalciuric Effect of Recombinant PTH in Patients with Activating Mutations of the Calcium-Sensing Receptor Causing Autosomal Dominant Hypocalcaemia-Hypercalciuria (ADHH)
FP10-2 Patients With Mutations In Phex Or FGF23 Share FGF23 Excess But Present Distinct BONE and Mineral Metabolism Features
FP25-6 Methylation and Transcripts Expression of GNAS Locus in Human iPSC and Their Differenciated Derivatives