Pages that link to "Q34474098"

The following pages link to Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing (Q34474098):

Displaying 11 items.

• In silico prediction of physical protein interactions and characterization of interactome orphans (Q24306744) (← links)
• SRMA: an R package for resequencing array data analysis (Q34267257) (← links)
• High-quality DNA sequence capture of 524 disease candidate genes (Q34835141) (← links)
• Coordinated regulation of mitochondrial topoisomerase IB with mitochondrial nuclear encoded genes and MYC. (Q35174664) (← links)
• The interface of transcription and DNA replication in the mitochondria (Q35907097) (← links)
• Rare variant detection using family-based sequencing analysis (Q36673312) (← links)
• APE2 is required for ATR-Chk1 checkpoint activation in response to oxidative stress. (Q36967831) (← links)
• The peroxisomal Lon protease LonP2 in aging and disease: functions and comparisons with mitochondrial Lon protease LonP1 (Q37507163) (← links)
• Mitochondrial DNA depletion syndrome: new descriptions and the use of citrate synthase as a helpful tool to better characterise the patients. (Q53145265) (← links)
• Isoforms of Base Excision Repair Enzymes Produced by Alternative Splicing (Q91657262) (← links)
• MUTYH: Not just polyposis (Q98613556) (← links)