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[Autosomal dominant (familial) infantile myofibromatosis: The causative role of mutations in PDGFRB and NOTCH3].

AuthorsO Dereure
JournalAnnales de dermatologie et de venereologie (Ann Dermatol Venereol) Vol. 140 Issue 12 Pg. 833-4 (Dec 2013) ISSN: 0151-9638 [Print] France
Vernacular TitleMyofibromatose infantile familiale autosomique dominante: responsabilité de mutations de PDGFRB et NOTCH3.
PMID24315235 (Publication Type: Journal Article, Comment)
Chemical References
  • Receptor, Platelet-Derived Growth Factor beta
Topics
  • Female
  • Genes, Dominant
  • Humans
  • Male
  • Mutation, Missense
  • Myofibromatosis (congenital)
  • Receptor, Platelet-Derived Growth Factor beta (genetics)

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