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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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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: 2009-05-07
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 431931
ISI: 000265910300037
 Degree: -

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Title: Blood
  Alternative Title : Blood
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 113 (19) Sequence Number: - Start / End Page: 4740 - 4746 Identifier: ISSN: 0006-4971