US EditionPublished • loading... • Updated
Identification of a Novel MYO1D Variant Associated with Laterality Defects, Congenital Heart Diseases, and Sperm Defects in Humans
Summary by Newswise
This story is only covered by news sources that have yet to be evaluated by the independent media monitoring agencies we use to assess the quality and reliability of news outlets on our platform. Learn more here.1 Articles
1 Articles
Identification of a Novel MYO1D Variant Associated with Laterality Defects, Congenital Heart Diseases, and Sperm Defects in Humans
Researchers from the Second Xiangya Hospital of Central South University, et al. have conducted a paper entitled "Identification of a novel MYO1D variant associated with laterality defects, congenital heart diseases, and sperm defects in humans". This study was published in Frontiers of Medicine, Volume 18, Issue 3.
·Charlottesville, United States
Read Full ArticleCoverage Details
Total News Sources1
Leaning Left0Leaning Right0Center0Last UpdatedBias DistributionNo sources with tracked biases.
Bias Distribution
- There is no tracked Bias information for the sources covering this story.
Factuality
To view factuality data please Upgrade to Premium
