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

BORIS DOI
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.
Date of Publication
2012
Publication Type
Article
Language(s)
en
Contributor(s)
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
Additional Credits
Series
Nephrology, dialysis, transplantation
Publisher
Oxford University Press
ISSN
0931-0509
ISBN
0931-0509
Access(Rights)
open.access
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