Article ID Journal Published Year Pages File Type
5589089 European Journal of Medical Genetics 2017 5 Pages PDF
Abstract
It was understood that after finding this mutation, when bone mineral density was measured with DXA in the family whose ages range between 19 and 28 and who have no bone problem before, osteoporosis was diagnosed. It was also understood that microphthalmia found in this family is a clinical finding of OPPG syndrome.
Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Genetics
Authors
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