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. |
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Zdroj: | Journal of Pediatric Endocrinology & Metabolism; Jul2005, Vol. 18 Issue 7, p689-699, 11p |
Databáze: | Complementary Index |
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