Familial Hypomagnesemia, Hypercalciuria and Nephrocalcinosis with Novel Mutation

Eitemau Tebyg

• Familial hypomagnesemia, hypercalciuria and nephrocalcinosis with novel mutation
  gan: S Margabandhu, et al.
  Cyhoeddwyd: (2019-01-01)
• Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis
  gan: García‐Castaño, Alejandro, et al.
  Cyhoeddwyd: (2020)
• Atypical presentation of familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a patient with a new claudin-16 gene mutation
  gan: Vianna, Júlia Guasti P., et al.
  Cyhoeddwyd: (2019)
• Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis
  gan: Claverie-Martín, Félix, et al.
  Cyhoeddwyd: (2013)
• Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC): Report of three cases with a novel mutation in CLDN19 gene
  gan: Amar Al-Shibli, et al.
  Cyhoeddwyd: (2013-01-01)