Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm

Lindsay, ME (author)

Schepers, D (author)

Bolar, NA (author)

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Doyle, JJ (author)

Gallo, E (author)

Fert-Bober, J (author)

Kempers, MJE (author)

Fishman, EK (author)

Chen, YC (author)

Myers, L (author)

Bjeda, D (author)

Oswald, G (author)

Elias, AF (author)

Levy, HP (author)

Anderlid, BM (author)

Karolinska Institutet

Yang, MH (author)

Bongers, EMHF (author)

Timmermans, J (author)

Braverman, AC (author)

Canham, N (author)

Mortier, GR (author)

Brunner, HG (author)

Byers, PH (author)

Van Eyk, J (author)

Van Laer, L (author)

Dietz, HC (author)

Loeys, BL (author)

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 (creator_code:org_t)

2012-07-08

2012

English.

In: Nature genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 44:8, s. 922-

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• Journal article (peer-reviewed)