Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Waleed Altay"'
Autor:
Amar Al-Shibli, Martin Konrad, Waleed Altay, Omar Al Masri, Lihad Al-Gazali, Ibrahim Al Attrach
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 24, Iss 2, Pp 338-344 (2013)
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is a rare autosomal recessive disorder that is caused by mutation in the genes coding for tight junction proteins Claudin-16 and Claudin-19. Affected individuals usually develop
Externí odkaz:
https://doaj.org/article/cd21bb92f8954875baaad98d42cd9faf
Autor:
Omar Al Masri, Amar Al-Shibli, Lihad Al-Gazali, Martin Konrad, Waleed Altay, Ibrahim Al Attrach
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 24, Iss 2, Pp 338-344 (2013)
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is a rare autosomal recessive disorder that is caused by mutation in the genes coding for tight junction proteins Claudin-16 and Claudin-19. Affected individuals usually develop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfd61a3fbef806d7eefbe8f986b895fc
https://doi.org/10.4103/1319-2442.109601
https://doi.org/10.4103/1319-2442.109601