Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis (FHHNC): Compound heterozygous mutation in the claudin 16 (CLDN16) gene

Lignende værker

• Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis
  af: García‐Castaño, Alejandro, et al.
  Udgivet: (2020)
• Two novel mutations of the CLDN16 gene cause familial hypomagnesaemia with hypercalciuria and nephrocalcinosis
  af: Hanssen, Oriane, et al.
  Udgivet: (2014)
• A novel CLDN16 mutation in a large family with familial hypomagnesaemia with hypercalciuria and nephrocalcinosis
  af: Deeb, Asma, et al.
  Udgivet: (2013)
• Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC): Report of three cases with a novel mutation in CLDN19 gene
  af: Amar Al-Shibli, et al.
  Udgivet: (2013-01-01)
• CLDN16 Genotype Predicts Renal Decline in Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis
  af: Konrad, Martin, et al.
  Udgivet: (2008)