Whole-exome sequencing identified a homozygous BRDT mutation in a patient with acephalic spermatozoa-Reference-Cited by-同舟云学术

Whole-exome sequencing identified a homozygous BRDT mutation in a patient with acephalic spermatozoa

Published:2017-02-10 Issue:12 Volume:8 Page:19914-19922
ISSN:1949-2553
Container-title:Oncotarget
language:en
Short-container-title:Oncotarget

Author:

Li Lin¹,Sha Yanwei²,Wang Xi³,Li Ping²,Wang Jing⁴,Kee Kehkooi¹,Wang Binbin³

Affiliation:

1. Center for Stem Cell Biology and Regenerative Medicine, Department of Basic Medical Sciences, School of Medicine, Tsinghua University, Beijing, 100084, China

2. Reproductive Medicine Center, Xiamen Maternal and Child Health Care Hospital, Xiamen, 361005, Fujian Province, China

3. Center for Genetics, National Research Institute for Family Planning, Haidian, Beijing, 100081, China

4. Department of Medical Genetics and Developmental Biology, School of Basic Medical Sciences, Capital Medical University, Beijing, 100069, China

Publisher

Impact Journals, LLC

Subject

Oncology

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