A family with autosomal dominant hypocalcaemia with hypercalciuria (ADHH): mutational analysis, phenotypic variability and treatment challenges.
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| Title: | A family with autosomal dominant hypocalcaemia with hypercalciuria (ADHH): mutational analysis, phenotypic variability and treatment challenges. |
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| Authors: | Burren CP; Department of Paediatric Endocrinology, Bristol Royal Hospital for Children, United Bristol Healthcare NHS Trust, Bristol, Avon, UK. Christine.Burren@ubht.swest.nhs.uk, Curley A, Christie P, Rodda CP, Thakker RV |
| Source: | Journal of pediatric endocrinology & metabolism : JPEM [J Pediatr Endocrinol Metab] 2005 Jul; Vol. 18 (7), pp. 689-99. |
| Publication Type: | Case Reports; Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Walter de Gruyter Country of Publication: Germany NLM ID: 9508900 Publication Model: Print Cited Medium: Print ISSN: 0334-018X (Print) Linking ISSN: 0334018X NLM ISO Abbreviation: J Pediatr Endocrinol Metab Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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