Article Versions Notes

Martín-Núñez E, Donate-Correa J, Kannengiesser C, De Brauwere D-P, Leroy C, Oudin C, Friedlander G, Prieto-Morín C, Tagua VG, Ureña-Torres PA, et al. A Novel Heterozygous Deletion Variant in KLOTHO Gene Leading to Haploinsufficiency and Impairment of Fibroblast Growth Factor 23 Signaling Pathway. Journal of Clinical Medicine. 2019; 8(4):500. https://doi.org/10.3390/jcm8040500

Martín-Núñez, Ernesto, Javier Donate-Correa, Caroline Kannengiesser, David-Paul De Brauwere, Christine Leroy, Claire Oudin, Gérard Friedlander, Carol Prieto-Morín, Víctor G. Tagua, Pablo A. Ureña-Torres, and et al. 2019. "A Novel Heterozygous Deletion Variant in KLOTHO Gene Leading to Haploinsufficiency and Impairment of Fibroblast Growth Factor 23 Signaling Pathway" Journal of Clinical Medicine 8, no. 4: 500. https://doi.org/10.3390/jcm8040500

Martín-Núñez, E., Donate-Correa, J., Kannengiesser, C., De Brauwere, D.-P., Leroy, C., Oudin, C., Friedlander, G., Prieto-Morín, C., Tagua, V. G., Ureña-Torres, P. A., & Navarro-González, J. F. (2019). A Novel Heterozygous Deletion Variant in KLOTHO Gene Leading to Haploinsufficiency and Impairment of Fibroblast Growth Factor 23 Signaling Pathway. Journal of Clinical Medicine, 8(4), 500. https://doi.org/10.3390/jcm8040500