MERRF (MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED RED FIBRES), MUTATION DETECTION

  • Test Usage:
    The MERRF syndrome is caused by a maternally-inherited mutation at position 8344 in the mitochondrial genome in over 80% of cases. This point mutation disrupts the mitochondrial gene for tRNA-Lys and so disrupts synthesis of proteins essential for oxidative phosphorylation. Many genes are involved which include MT-TK, MT-TL1, MT-TH, MT-TS1., MT-TS2, MT-TF etc.
  • Report Availability:
    Sample Daily by 11 am; Report 10 days
4 Diagnostic Centers found for MERRF (MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED RED FIBRES), MUTATION DETECTION in Ahmedabad
  • Shop No.1, Savan Apt, Opp.B-2 Surjit, Naran Chamber Lane, Thakkar Nagar Bapunagar Road, India Colony, Bapu Nagar


    8849210244

    akyagnik09@gmail.com

    Collection Center
  • 286/SOBO Center, South Bopal, Bopal, Ahmedabad, Gujarat


    9723214970

    dp014560@gmail.com

    Collection Center
  • A/7, Basement Of K.B.Complex, Dairy Road, Below Balaji Hospital, Mahesana, Gujarat-384002


    9737182440

    hitech33@gmail.com

    Collection Center
  • 3-Abhikram Complex, Near Home Town Furniture Mall, Opposite Bhaikaka Nagar, Thaltej, Ahmedabad-380059


    079 26859105, 9824065920, 8488081642

    neeteen440u@yahoo.co.in

    Collection Center