Osteopetrosis and Its Relevance for the Discovery of New Functions Associated with the Skeleton
Osteopetrosis is a rare genetic disorder characterized by an increase of bone mass due to defective osteoclast function. Patients typically displayed spontaneous fractures, anemia, and in the most severe forms hepatosplenomegaly and compression of cranial facial nerves leading to deafness and blindn...
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| Huvudupphov: | , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Utgiven: |
Wiley
2015-01-01
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| Serie: | International Journal of Endocrinology |
| Länkar: | http://dx.doi.org/10.1155/2015/372156 |
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