PubMed 23307537
Referenced in: none
Automatically associated channels: Kir2.3 , Kir6.2 , Kv2.1
Title: Wide clinical variability in conditions with coarse facial features and hypertrichosis caused by mutations in ABCC9.
Authors: Johanna Christina Czeschik, Claudia Voigt, Timm O Goecke, Hermann-Josef Lüdecke, Nicholas Wagner, Alma Kuechler, Dagmar Wieczorek
Journal, date & volume: Am. J. Med. Genet. A, 2013 Feb , 161A, 295-300
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/23307537
Abstract