Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy
1p36 缺失综合征的精细定位确定 PRDM16 突变是心肌病的病因
期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2013.05.015
Anne-Karin Arndt, Sebastian Schafer, Jorg-Detlef Drenckhahn, M Khaled Sabeh, Eva R Plovie, Almuth Caliebe, Eva Klopocki, Gabriel Musso, Andreas A Werdich, Hermann Kalwa, Matthias Heinig, Robert F Padera, Katharina Wassilew, Julia Bluhm, Christine Harnack, Janine Martitz, Paul J Barton, Matthias Greu