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Published in 2018 at "Clinical Oral Investigations"
DOI: 10.1007/s00784-018-2496-9
Abstract: ObjectivesCleidocranial dysplasia (CCD) is a rare autosomal-dominantly inherited skeletal dysplasia that is predominantly associated with heterozygous mutations of RUNX2. However, no information is available regarding metabolic changes associated with CCD at present.Materials and methodsWe analyzed…
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Keywords:
ccd;
profiling cleidocranial;
metabolomics profiling;
dysplasia ... See more keywords