Identification of a novel TGFBR1 mutation in a Loeys-Dietz syndrome type II patient with vascular Ehlers-Danlos syndrome phenotype [2]

B. Drera, G. Tadini, S. Barlati, M. Colombi

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)290-293
Number of pages4
JournalClinical Genetics
Volume73
Issue number3
DOIs
Publication statusPublished - Mar 2008

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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