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 journal › Article

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 journal › Article

Drera, B, Tadini, G, Barlati, S & Colombi, M 2008, 'Identification of a novel TGFBR1 mutation in a Loeys-Dietz syndrome type II patient with vascular Ehlers-Danlos syndrome phenotype [2]', Clinical Genetics, vol. 73, no. 3, pp. 290-293. https://doi.org/10.1111/j.1399-0004.2007.00942.x
Drera B, Tadini G, Barlati S, Colombi M. Identification of a novel TGFBR1 mutation in a Loeys-Dietz syndrome type II patient with vascular Ehlers-Danlos syndrome phenotype [2]. Clinical Genetics. 2008 Mar;73(3):290-293. https://doi.org/10.1111/j.1399-0004.2007.00942.x
Drera, B. ; Tadini, G. ; Barlati, S. ; Colombi, M. / Identification of a novel TGFBR1 mutation in a Loeys-Dietz syndrome type II patient with vascular Ehlers-Danlos syndrome phenotype [2]. In: Clinical Genetics. 2008 ; Vol. 73, No. 3. pp. 290-293.
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