Molecular and clinical genetic studies of a novel variant of familial hypercalcemia
Familial primary hyperparathyroidism (HPT) is a rare disorder that is treated surgically and mostly occurs in association with tumor-susceptibility syndromes, like multiple endocrine neoplasia and the hyperparathyroidism-jaw tumor syndrome. Familial hypercalciuric hypercalcemia (FHH) is another caus...
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| Format: | Doctoral Thesis |
| Language: | English |
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Uppsala universitet, Institutionen för kirurgiska vetenskaper, Uppsala, Sweden
2002
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| Online Access: | http://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-57632 http://nbn-resolving.de/urn:isbn:91-554-5300-7 |