CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT)

Abstract Background. Recently, we identified a microduplication in chromosomal band 1q21.1 encompassing the CHD1L/ALC1 gene encoding a chromatin-remodelling e

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Bibliographic Details
Main Authors: Brockschmidt, Antje (Author) , Schaefer, Franz (Author)
Format: Article (Journal)
Language:English
Published: 2012
In: Nephrology, dialysis, transplantation
Year: 2011, Volume: 27, Issue: 6, Pages: 2355-2364
ISSN:1460-2385
DOI:10.1093/ndt/gfr649
Online Access:Verlag, kostenfrei, Volltext: http://dx.doi.org/10.1093/ndt/gfr649
Verlag, kostenfrei, Volltext: https://academic.oup.com/ndt/article/27/6/2355/1941432
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Author Notes:Antje Brockschmidt, Boidinh Chung, Stefanie Weber, Dagmar-Christiane Fischer, Maria Kolatsi-Joannou, Laura Christ, André Heimbach, Diamant Shtiza, Günter Klaus, Giacomo D. Simonetti, Martin Konrad, Paul Winyard, Dieter Haffner, Franz Schaefer and Ruthild G. Weber
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Summary:Abstract Background. Recently, we identified a microduplication in chromosomal band 1q21.1 encompassing the CHD1L/ALC1 gene encoding a chromatin-remodelling e
Item Description:Advance access publication 6 December 2011
Gesehen am 06.08.2018
Physical Description:Online Resource
ISSN:1460-2385
DOI:10.1093/ndt/gfr649