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  Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissections

Hoffjan, S., Waldmüller, S., Blankenfeldt, W., Kötting, J., Gehle, P., Binner, P., et al. (2011). Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissections. European Journal of Human Genetics, 19(5): 1, pp. 520-524. Retrieved from http://dx.doi.org/10.1038/ejhg.2010.239.

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 Creators:
Hoffjan, Sabine, Author
Waldmüller, Stephan, Author
Blankenfeldt, Wulf1, Author           
Kötting, Judith, Author
Gehle, Petra, Author
Binner, Priska, Author
Epplen, Joerg T., Author
Scheffold, Thomas, Author
Affiliations:
1Abt. III: Physikalische Biochemie, Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753289              

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Free keywords: ACTA2; marfan syndrome; TAAD; aneurysm; dissection; actin
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Language(s): eng - English
 Dates: 2011
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 563643
URI: http://dx.doi.org/10.1038/ejhg.2010.239
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Title: European Journal of Human Genetics
Source Genre: Journal
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Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 19 (5) Sequence Number: 1 Start / End Page: 520 - 524 Identifier: -