CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT)
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BORIS DOI
Date of Publication
2012
Publication Type
Article
Division/Institute
Contributor
Brockschmidt, Antje | |
Chung, Boidinh | |
Weber, Stefanie | |
Fischer, Dagmar-Christiane | |
Kolatsi-Joannou, Maria | |
Christ, Laura | |
Heimbach, André | |
Shtiza, Diamant | |
Klaus, Günter | |
Konrad, Martin | |
Winyard, Paul | |
Haffner, Dieter | |
Schaefer, Franz | |
Weber, Ruthild G |
Series
Nephrology, dialysis, transplantation
ISSN or ISBN (if monograph)
0931-0509
Publisher
Oxford University Press
Language
English
Publisher DOI
PubMed ID
22146311
Description
Recently, we identified a microduplication in chromosomal band 1q21.1 encompassing the CHD1L/ALC1 gene encoding a chromatin-remodelling enzyme in congenital anomalies of the kidneys and urinary tract (CAKUT) patient.
File(s)
| File | File Type | Format | Size | License | Publisher/Copright statement | Content | |
|---|---|---|---|---|---|---|---|
| gfr649.pdf | text | Adobe PDF | 1.5 MB | publisher | published |