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Analysis of mutations in the SOS-1 gene in two Polish families with hereditary gingival fibromatosis.

Katarzyna GawronG BeretaZ NowakowskaK Łazarz-BartyzelJ PotempaM Chomyszyn-GajewskaR GórskaP Plakwicz
Published in: Oral diseases (2017)
Patients from two Polish families under study had not been affected by hereditary gingival fibromatosis type 1, caused by a single-cytosine insertion in exon 21 of the Son-of-Sevenless-1 gene. Further studies of the remaining regions of this gene as well as of other genes are needed to identify disease-related mutations in these patients. This will help to unravel the pathogenic mechanism of gingival overgrowth.
Keyphrases
  • genome wide
  • ejection fraction
  • newly diagnosed
  • copy number
  • prognostic factors
  • dna methylation
  • patient reported
  • drug induced