Correction: Bi-allelic loss of function variants in SLC30A5 as cause of perinatal lethal cardiomyopathy.

著录项

• 来源
  《European journal of human genetics: EJHG》 |2021年第5期|共1页
• 作者

  Johann Kaspar Lieberwirth; Pascal Joset; Anja Heinze; Julia Hentschel; Anja Stein; Antonella Iannaccone; Katharina Steindl; Alma Kuechler; Rami Abou Jamra;

  展开▼
• 作者单位

  Institute of Human Genetics University Medical Center Leipzig;

  Institute of Medical Genetics University of Zurich;

  Institute of Human Genetics University Medical Center Leipzig;

  Institute of Human Genetics University Medical Center Leipzig;

  Department of Pediatrics I Division of Neonatology University Medical Center Essen University;

  Department of Gynecology and Obstetrics University Medical Center Essen University Duisburg-Essen;

  Institute of Medical Genetics University of Zurich;

  Institute of Human Genetics University Medical Center Essen University of Duisburg-Essen;

  Institute of Human Genetics University Medical Center Leipzig;

  展开▼
• 收录信息
• 原文格式 PDF
• 正文语种 eng
• 中图分类 医学遗传学;
• 关键词