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  Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein

van Wijk, E., Kersten, F. F. J., Kartono, A., Mans, D. A., Brandwijk, K., Letteboer, S. J. F., et al. (2009). Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein. Human Molecular Genetics, 18(1), 51-64.

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Genre: Journal Article
Alternative Title : Hum. Mol. Genet.

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 Creators:
van Wijk, E., Author
Kersten, F. F. J., Author
Kartono, A., Author
Mans, D. A., Author
Brandwijk, K., Author
Letteboer, S. J. F., Author
Peters, T. A., Author
Marker, T., Author
Yan, X. M.1, Author           
Cremers, C. W. R. J., Author
Cremers, F. P. M., Author
Wolfrum, U., Author
Roepman, R., Author
Kremer, H., Author
Affiliations:
1Former Research Groups, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565145              

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Language(s): eng - English
 Dates: 2009-01-01
 Publication Status: Published in print
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 397237
ISI: 000261680300005
 Degree: -

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Title: Human Molecular Genetics
  Alternative Title : Hum. Mol. Genet.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 18 (1) Sequence Number: - Start / End Page: 51 - 64 Identifier: ISSN: 0964-6906