Validation of low-coverage whole-genome sequencing for mitochondrial DNA variants suggests mitochondrial DNA as a genetic cause of preterm birth.

Authors:
Yang Z; Slone J; Wang X; Zhan J; Huang Y and 7 more

Journal:
Hum Mutat

Publication Year: 2021

DOI:
10.1002/humu.24279

PMCID:
PMC9290920

PMID:
34467602

Journal Information

Full Title: Hum Mutat

Abbreviation: Hum Mutat

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Genetics, Medical

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

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2/6
0.0% Transparent
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Evidence found in paper:

"CONFLICT OF INTERESTS The authors declare that there is no conflict of interests."

Evidence found in paper:

"We wish to thank our collaborators and the patient participants for their contributions to this study. This study used samples, data, and/or services from the Discover Together Biobank at Cincinnati Children's Research Foundation. We thank the Discover Together Biobank for support of this study, as well as participants and their families, whose help and participation made this work possible. The study was supported in part by the Cincinnati Children's Hospital Research Foundation (TH)."

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Open Access
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Last Updated: Aug 05, 2025