Intrafamilial variability of cardiovascular abnormalities associated with the p.R460H mutation of the TGFBR2 gene

Pol Arch Intern Med. 2020 Aug 27;130(7-8):676-678. doi: 10.20452/pamw.15365. Epub 2020 May 18.
No abstract available

MeSH terms

  • Cardiovascular Abnormalities*
  • Humans
  • Mutation
  • Receptor, Transforming Growth Factor-beta Type II / genetics

Substances

  • Receptor, Transforming Growth Factor-beta Type II