LAD-1/variant syndrome is caused by mutations in FERMT3

Kuijpers, T. W.; van de Vijver, E.; Weterman, M. A. J.; de Boer, M.; Tool, A. T. J.; van den Berg, T. K.; Moser, M.; Jakobs, M. E.; Seeger, K.; Sanal, O.; Unal, S.; Cetin, M.; Roos, D.; Verhoeven, A. J.; Baas, F.

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LAD-1/variant syndrome is caused by mutations in FERMT3

Kuijpers, T. W., van de Vijver, E., Weterman, M. A. J., de Boer, M., Tool, A. T. J., van den Berg, T. K., et al. (2009). LAD-1/variant syndrome is caused by mutations in FERMT3. Blood, 113(19), 4740-4746.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0010-59B6-8 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0010-59B7-6

Genre: Journal Article

Alternative Title : Blood

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Creators:
Kuijpers, T. W., Author
van de Vijver, E., Author
Weterman, M. A. J., Author
de Boer, M., Author
Tool, A. T. J., Author
van den Berg, T. K., Author
Moser, M.¹, Author
Jakobs, M. E., Author
Seeger, K., Author
Sanal, O., Author
Unal, S., Author
Cetin, M., Author
Roos, D., Author
Verhoeven, A. J., Author
Baas, F., Author

Affiliations:
1Fässler, Reinhard / Molecular Medicine, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565147

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Language(s): eng - English

Dates: Date issued: 2009-05-07

Publication Status: Issued

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Rev. Type: Peer

Identifiers: eDoc: 431931
ISI: 000265910300037

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Title: Blood

Alternative Title : Blood

Source Genre: Journal

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Pages: - Volume / Issue: 113 (19) Sequence Number: - Start / End Page: 4740 - 4746 Identifier: ISSN: 0006-4971