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; Jul2005, Vol. 18 Issue 7, p689-699, 11p
Databáze: Complementary Index