ArticleCalcified tissue international2024

Identification of a Novel Homozygous Missense Mutation in the CLDN16 Gene to Decipher the Ambiguous Clinical Presentation Associated with Autosomal Dominant Hypocalcaemia and Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis in an Indian Family.

Rupesh Thapa et al.PubMed ↗Publisher ↗

No numbers read from the abstract.