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  Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux

Marcil, M., Brooks-Wilson, A., Clee, S. M., Roomp, K., Zhang, L.-H., Yu, L., et al. (1999). Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux. The Lancet, 354(9187), 1341-6.

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 Creators:
Marcil, Michel, Author
Brooks-Wilson, A., Author
Clee, Susanne M., Author
Roomp, Kirsten1, Author           
Zhang, Lin-Hua, Author
Yu, L., Author
Collins, Jennifer A., Author
van Dam, M., Author
Molhuizen, H. O., Author
Loubser, O., Author
Ouelette, B. F., Author
Sensen, C. W., Author
Fichter, K., Author
Mott, S., Author
Denis, M., Author
Boucher, B., Author
Pimstone, S., Author
Genest, Jacques, Author
Kastelein, J. J. P., Author
Hayden, Michael R., Author
Affiliations:
1Computational Biology and Applied Algorithmics, MPI for Informatics, Max Planck Society, ou_40046              

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Language(s): eng - English
 Dates: 2010-12-061999
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 520888
Other: Local-ID: C125673F004B2D7B-81D87C8611E25B5CC1256CF3004F0D7F-Roomp1999b
 Degree: -

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Title: The Lancet
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 354 (9187) Sequence Number: - Start / End Page: 1341 - 6 Identifier: -