Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Jacqueline, Vekich"'
Autor:
Rachel Roach, Joseph Sergi, Mark Horn, Mike Favis, Jeanne Sue Magram, Victoria Markiewicz, William B. Snyder, Kymberly Levine, Jennifer Colangelo, Jean Chamoun, Moosa Mohammadi, Jacqueline Vekich, Dikran Aivazian, Edwin Berryman, William J. Reagan, Cedo M. Bagi, Kristen Johnson, Anthony J. Coyle, Brian Robert Miller, Xianjun Cao, Thomas P. Brown
Publikováno v:
Journal of Bone and Mineral Research. 32:2062-2073
Fibroblast growth factor 23 (FGF23) is the causative factor of X-linked hypophosphatemia (XLH), a genetic disorder effecting 1:20,000 that is characterized by excessive phosphate excretion, elevated FGF23 levels and a rickets/osteomalacia phenotype.
Autor:
Kristen, Johnson, Kymberly, Levine, Joseph, Sergi, Jean, Chamoun, Rachel, Roach, Jacqueline, Vekich, Mike, Favis, Mark, Horn, Xianjun, Cao, Brian, Miller, William, Snyder, Dikran, Aivazian, William, Reagan, Edwin, Berryman, Jennifer, Colangelo, Victoria, Markiewicz, Cedo M, Bagi, Thomas P, Brown, Anthony, Coyle, Moosa, Mohammadi, Jeanne, Magram
Publikováno v:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 32(10)
Fibroblast growth factor 23 (FGF23) is the causative factor of X-linked hypophosphatemia (XLH), a genetic disorder effecting 1:20,000 that is characterized by excessive phosphate excretion, elevated FGF23 levels and a rickets/osteomalacia phenotype.