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

doi:10.1111/j.1399-0004.2007.00942.x

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

Fondazione IRCCS Ca' Granda- Ospedale Maggiore Policlinico

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	290-293
Number of pages	4
Journal	Clinical Genetics
Volume	73
Issue number	3
DOIs	https://doi.org/10.1111/j.1399-0004.2007.00942.x
Publication status	Published - Mar 2008

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1111/j.1399-0004.2007.00942.x

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author = "B. Drera and G. Tadini and S. Barlati and M. Colombi",

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

ASJC Scopus subject areas

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