A Case of Autosomal Dominant Osteopetrosis Type 2 with a CLCN7 Gene Mutation
Osteopetrosis is a rare genetic disease characterized by increased bone density and bone fractures due to defective osteoclast function. Autosomal dominant osteopetrosis type 2 (ADO-2), Albers-Schonberg disease, is characterized by the sclerosis of bones, predominantly involving the spine, pelvis an...
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| Main Authors: | , , , , |
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| Format: | Book |
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Galenos Yayincilik,
2019-12-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |