Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12) DNA test lab cost 45000.00 /- Rs

Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12) DNA Test

Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12)

Leave Message

Reporting Time: 5 Week
Test Cost: 45000.00 /- Rs
Sample Type: EDTA blood or DNA
Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12) Test Description Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12) Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12) genetic dna test for Neurological Diseases testing done with next gene sequencing NGS sample type Blood or DNA and reporing time is 4 to 5 weeks

Rating: 5

Total votes: 1

Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12) TEST DETAILS

Deatils about the test Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12)
  • What is the cost of Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12) ?
  • The cost of the Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12) is 45000.00/- Rs
  • How long will it take to get the reports and results for Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12) ?
  • The total time taken to get the results and reports for the Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12) would be 5 Week
  • will you collect sample from home for Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12) ?
  • Yes the sample will be collected from home for this Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12) for free of cost from Delhi, Mumbai, Kolkata Chennai, Bnaglaore, Hyderabad, ahmedabad and pune. For other cities mostly its free even if they charge its negligible fees.
  • How can we make the payment for this Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12) ?
  • You can make the payment online and through debit card, credit card & net banking for Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12). If you are making payment through cheque or demand draft (DD), then it must be in the favor of DNA Labs India. For cash payments you will get cash receipt
  • How accurate and quality are Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12) results
  • all Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12) samples are processed twice in order to double-check the result. In this way you can have absolute confidence that the result you receive is accurate and correct.
FOR ALL ONLINE PAYMENTS for Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12) 100% FREE HOME COLLECTION

It is very easy to order a Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12). It is safe, secure, confidential and best of all, an easy process. Avoid the hassle of one day off from your work , Traffic , Pollution. Our Highly Qualified Phlebotomist will Visit your Home for Sample Collection as per your Convenient Time slot booked by you.

Our streamlined services help you get the required health information directly to you quickly, efficiently, and professionally with doorstep Service and report delivery.

  • Make the payment Online for Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12)
  • Fill the Form with your details for Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12)
  • You will receive call from us
  • Schedule a appointment time for Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12)
  • Free home collection for Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12)
  • Receive reports online for Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12)
  • Hardcopy delivered to you in 24 hrs for Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12)
  • Save your Money and Time with us for Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12)
  • Easy and Affordable Billing for Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12)
  • 100% money back guaranty for Leigh syndrome due to mitochondrial complex I deficiency (NDUFA12)