Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations

類似資料

• Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis
  著者:: García‐Castaño, Alejandro, 等
  出版事項: (2020)
• CLDN16 Genotype Predicts Renal Decline in Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis
  著者:: Konrad, Martin, 等
  出版事項: (2008)
• Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis: Phenotype–Genotype Correlation and Outcome in 32 Patients with CLDN16 or CLDN19 Mutations
  著者:: Godron, Astrid, 等
  出版事項: (2012)
• Familial hypomagnesemia, hypercalciuria and nephrocalcinosis with novel mutation
  著者:: S Margabandhu, 等
  出版事項: (2019-01-01)
• Familial Hypomagnesemia, Hypercalciuria and Nephrocalcinosis with Novel Mutation
  著者:: Margabandhu, S., 等
  出版事項: (2019)