Title : Phenotypic features of dentinogenesis imperfecta associated with osteogenesis imperfecta and COL1A2 mutations.

Pub. Date : 2021 Jun

PMID : 33737018






1 Functional Relationships(s)
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1 RESULTS: All patients were identified with heterozygous glycine substitutions in COL1A2. Glycine collagen type I alpha 2 chain Homo sapiens