Literature DB >> 32317151

Clinical utility of whole genome sequencing for the detection of mitochondrial genome mutations.

Ammar Husami1, Jesse Slone1, Jenice Brown1, Meghan Bromwell1, C Alexander Valencia2, Taosheng Huang3.   

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Year:  2020        PMID： 32317151     DOI： 10.1016/j.jgg.2020.03.001

Source DB:  PubMed          Journal:  J Genet Genomics        ISSN： 1673-8527            Impact factor:   4.275


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  1 in total

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

Authors:  Zeyu Yang; Jesse Slone; Xinjian Wang; Jack Zhan; Yongbo Huang; Bahram Namjou; Kenneth M Kaufman; Michael Pauciulo; John B Harley; Louis J Muglia; Iouri Chepelev; Taosheng Huang
Journal:  Hum Mutat       Date:  2021-09-08       Impact factor: 4.700
  1 in total

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