Correction to: A homozygous FANCM frameshift pathogenic variant causes male infertility (Genetics in Medicine, (2019), 21, 1, (62-70), 10.1038/s41436-018-0015-7)

Hao Yin, Hui Ma, Sajjad Hussain, Huan Zhang, Xuefeng Xie, Long Jiang, Xiaohua Jiang, Furhan Iqbal, Ihtisham Bukhari, Hanwei Jiang, Asim Ali, Liangwen Zhong, Tao Li, Suixing Fan, Beibei Zhang, Jianing Gao, Yang Li, Jabeen Nazish, Teka Khan, Manan KhanMuhammad Zubair, Qiaomei Hao, Hui Fang, Jun Huang, Mahmoud Huleihel, Jiahao Sha, Tej K. Pandita, Yuanwei Zhang, Qinghua Shi

Research output: Contribution to journalComment/debate

6 Scopus citations

Abstract

Hao Win, Hui Ma and Sajjad Hussain were incorrectly affiliated to ‘Department of Radiation Oncology, The Houston Methodist Research Institute, Houston, TX 77030 USA’. These authors should only have been affiliated to ‘Hefei National Laboratory for Physical Sciences at Microscale, The First Affiliated Hospital of USTC, USTC-SJH Joint Center for Human Reproduction and Genetics, The CAS Key Laboratory of Innate Immunity and Chronic Diseases, School of Life Sciences, CAS Center for Excellence in Molecular Cell Science, Collaborative Innovation Center of Genetics and Development, University of Science and Technology of China, Hefei 230027, China’. They were also not noted as contributing equally to the paper. Both these errors have now been corrected in the PDF and HTML versions of the paper.

Original languageEnglish
Pages (from-to)266
Number of pages1
JournalGenetics in Medicine
Volume21
Issue number1
DOIs
StatePublished - 1 Jan 2019

ASJC Scopus subject areas

  • Genetics(clinical)

Fingerprint

Dive into the research topics of 'Correction to: A homozygous FANCM frameshift pathogenic variant causes male infertility (Genetics in Medicine, (2019), 21, 1, (62-70), 10.1038/s41436-018-0015-7)'. Together they form a unique fingerprint.

Cite this