Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features
Titel:
Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features
Auteur:
Eltan, Mehmet Yavas Abali, Zehra Turkyilmaz, Ayberk Gokce, Ibrahim Abali, Saygın Alavanda, Ceren Arman, Ahmet Kirkgoz, Tarik Guran, Tulay Hatun, Sukru Bereket, Abdullah Turan, Serap