A Family with Autosomal Dominant Hypocalcaemia with Hypercalciuria (ADHH): Mutational Analysis, Phenotypic Variability and Treatment Challenges

Autor: Burren, C.P., Curley, A., Christie, P., Rodda, C.P., Thakker, R.V.
Zdroj: Journal of Pediatric Endocrinology & Metabolism; July 2005, Vol. 18 Issue: 7 p689-700, 12p
Databáze: Supplemental Index