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Clinical Kidney Journal|August 5, 2024
Pathogenic heterozygous TRPM7 variants and hypomagnesemia with developmental delayWillem Bosman, Kameryn M Butler, Caitlin A Chang, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 13, 2022
Possible role for rare TRPM7 variants in patients with hypomagnesaemia with secondary hypocalcaemiaRosa Vargas-Poussou, Felix Claverie-Martin, Caroline Prot-Bertoye, et al.The Journal of Biological Chemistry|December 1, 2016
Structural Basis of the Oncogenic Interaction of Phosphatase PRL-1 with the Magnesium Transporter CNNM2Paula Giménez-Mascarell, Iker Oyenarte, Serge Hardy, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|February 28, 2018
URAT1 and GLUT9 mutations in Spanish patients with renal hypouricemiaFelix Claverie-Martin, Jorge Trujillo-Suarez, Hilaria Gonzalez-Acosta, et al.Journal of Pediatric Genetics|September 15, 2016
Dent's disease: Identification of seven new pathogenic mutations in the CLCN5 geneElena Ramos-Trujillo, Felix Claverie-Martin, Victor Garcia-Nieto, et al.Human Mutation|February 18, 2021
The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2)Gijs A C Franken, Dominik Müller, Cyril Mignot, et al.Pageof 3