Matches in Nanopublications for { ?s ?p "[A spontaneous novel mutation in COL1A2 (c.1171G>A; p.Gly391Ser) causing only dentin defects and a novel mutation in PAX9 (c.43T>A; p.Phe15Ile) causing hypodontia were identified and correlated with the phenotypic presentations in the family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 1 of
1
with 100 items per page.
- NP850046.RAMhslBVCtg_HFeM2zfjO9-ybI-r-m5nBf-Nhw6QBtNQA130_assertion description "[A spontaneous novel mutation in COL1A2 (c.1171G>A; p.Gly391Ser) causing only dentin defects and a novel mutation in PAX9 (c.43T>A; p.Phe15Ile) causing hypodontia were identified and correlated with the phenotypic presentations in the family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP850046.RAMhslBVCtg_HFeM2zfjO9-ybI-r-m5nBf-Nhw6QBtNQA130_provenance.