A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings.
Alparslan C, Öncel EP, Akbay S, Alaygut D, Mutlubaş F, Tatlı M, Konrad M, Yavaşcan Ö, Kasap-Demir B.
Alparslan C, et al. Among authors: konrad m.
Turk J Pediatr. 2018;60(1):76-80. doi: 10.24953/turkjped.2018.01.011.
Turk J Pediatr. 2018.
PMID: 30102483
Free article.
Alparslan C, Oncel EP, Akbay S, Alaygut D, Mutlubas F, Tatli M, Konrad M, Yavascan O, Kasap-Demir B. A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings. ...
Alparslan C, Oncel EP, Akbay S, Alaygut D, Mutlubas F, Tatli M, Konrad M, Yavascan O, Kasap-Demir B. A novel homozygous …