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

15 Citations (Scopus)
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)

Cite this

Identification of a novel TGFBR1 mutation in a Loeys-Dietz syndrome type II patient with vascular Ehlers-Danlos syndrome phenotype [2]. / Drera, B.; Tadini, G.; Barlati, S.; Colombi, M.

In: Clinical Genetics, Vol. 73, No. 3, 03.2008, p. 290-293.

Research output: Contribution to journalArticle

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