Clinical utility gene card for: familial hypomagnesemia with hypercalciuria and nephrocalcinosis with/without severe ocular involvement

Lignende værker

• Familial hypomagnesemia, hypercalciuria and nephrocalcinosis with novel mutation
  af: S Margabandhu, et al.
  Udgivet: (2019-01-01)
• Familial Hypomagnesemia, Hypercalciuria and Nephrocalcinosis with Novel Mutation
  af: Margabandhu, S., et al.
  Udgivet: (2019)
• Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis
  af: Claverie-Martín, Félix, et al.
  Udgivet: (2013)
• Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis
  af: García‐Castaño, Alejandro, et al.
  Udgivet: (2020)
• Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis: clinical and molecular characteristics
  af: Claverie-Martin, Felix
  Udgivet: (2015)