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  Structural and functional analysis of a novel mutation of CYP21B in a heterozygote carrier of 21-hydroxylase deficiency

Bojunga, J., Welsch, C., Antes, I., Albrecht, M., Lengauer, T., & Zeuzem, S. (2005). Structural and functional analysis of a novel mutation of CYP21B in a heterozygote carrier of 21-hydroxylase deficiency. Human Genetics, 117, 558-564.

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 Creators:
Bojunga, Jörg, Author
Welsch, Christoph1, Author           
Antes, Iris1, Author           
Albrecht, Mario1, Author           
Lengauer, Thomas1, Author           
Zeuzem, Stefan, Author
Affiliations:
1Computational Biology and Applied Algorithmics, MPI for Informatics, Max Planck Society, ou_40046              

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Language(s): eng - English
 Dates: 2006-01-172005
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 279098
Other: Local-ID: C125673F004B2D7B-2CF8636AA3233CE6C1256FEB0060FC3A-Antes2005d
 Degree: -

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Title: Human Genetics
Source Genre: Journal
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Publ. Info: -
Pages: - Volume / Issue: 117 Sequence Number: - Start / End Page: 558 - 564 Identifier: ISBN: 03406717