N. GÜLERAY LAFCI Et Al. , "Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria," European Journal of Human Genetics , 2024
GÜLERAY LAFCI, N. Et Al. 2024. Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria. European Journal of Human Genetics .
GÜLERAY LAFCI, N., van Goor, M., Cetinkaya, S., van der Wijst, J., Acun, M., Kurt Colak, F., ... ÇETİNKAYA, A.(2024). Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria. European Journal of Human Genetics .
GÜLERAY LAFCI, NAZ Et Al. "Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria," European Journal of Human Genetics , 2024
GÜLERAY LAFCI, NAZ G. Et Al. "Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria." European Journal of Human Genetics , 2024
GÜLERAY LAFCI, N. Et Al. (2024) . "Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria." European Journal of Human Genetics .
@article{article, author={NAZ GÜLERAY LAFCI Et Al. }, title={Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria}, journal={European Journal of Human Genetics}, year=2024}