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Mitochondrial genome associated with another NGS panel
Analysis of the 37 mtDNA genes and disease-associated variants.
For more information, please contact with us.
Request study
Informed consent
Steps to follow
Ask for information
Steps to follow
How to order
1. Download & fill out
Please cover as many fields as possible in both documents
2. Sample collection
Three sample types: saliva, peripheral blood or genomic DNA
3. Pack the sample
Please pack the sample in a way to prevent leakage
4. Send the sample & the request
Please schedule the delivery for Mon–Thur: 8am – 5pm
5. Result: the report
Via: Client Site HIC / Client Site Imegen / Certified email
Solicita información de
Mitochondrial genome associated with another NGS panel
Turnaround time (TAT): 6 weeks
Ref. S-201805390
Phenotypes
- Epilepsia mioclónica con fibras rojas rasgadas (MERRF)
- Miopatía mitocondrial con encefalopatía, acidosis láctica y episodios similares al ictus-like (MELAS)
- Neuropatía óptica hereditaria de Leber (LHON)
- Neuropatía, ataxia, retinitis pigmentaria (NARP)
- Oftalmoplejía externa progresiva crónica (CPEO)
- Síndrome de Kearns-Sayre
- Síndrome de Leigh
- Síndrome de Pearson