Two novel mutations in TCIRG1 induced infantile malignant osteopetrosis: a case report
Abstract Background Infantile malignant osteopetrosis (IMO) is a rare autosomal recessive disease characterized by a higher bone density in bone marrow caused by the dysfunction of bone resorption. Clinically, IMO can be diagnosed with medical examination, bone mineral density test and whole genome...
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Main Authors: | , , , , , , , , , , , , |
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Format: | Book |
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BMC,
2021-07-01T00:00:00Z.
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A1234.567 |
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