1. Clinical utility of whole genome sequencing for the detection of mitochondrial genome mutations. (20th March 2020) Authors: Husami, Ammar; Slone, Jesse; Brown, Jenice; Bromwell, Meghan; Valencia, C. Alexander; Huang, Taosheng Journal: Journal of genetics and genomics Issue: Volume 47:Number 3(2020) Page Start: 167 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Mitochondrial genome variant m.3250T>C as a possible risk factor for mitochondrial cardiomyopathy. Issue 2 (1st December 2020) Authors: Campbell, Teresa; Lou, Xiaoting; Slone, Jesse; Brown, Jenice; Bromwell, Meghan; Liu, Jie; Bai, Renkui; Haude, Katrina; Balog, Amanda; Cui, Hong; Zou, Weiwei; Yang, Li; Al‐Beshri, Ali; Huang, Taosheng Journal: Human mutation Issue: Volume 42:Issue 2(2021) Page Start: 177 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Mitochondrial genome variant m.3250T>C as a possible risk factor for mitochondrial cardiomyopathy. Issue 2 (1st December 2020) Authors: Campbell, Teresa; Lou, Xiaoting; Slone, Jesse; Brown, Jenice; Bromwell, Meghan; Liu, Jie; Bai, Renkui; Haude, Katrina; Balog, Amanda; Cui, Hong; Zou, Weiwei; Yang, Li; Al‐Beshri, Ali; Huang, Taosheng Journal: Human mutation Issue: Volume 42:Issue 2(2021) Page Start: 177 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗