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 Hyderabad
  • Robin Healthcare Solutions, Sri Lakshmi Nilayam, Mig286, Ground Floor, Opposite Global Edge School, Remedy Hospital Road, Road No4, KPHB, Kukatapally, Hyderabad, Telangana-500072


    8008852952

    robinhealthcaresolution@gmail.com

    Collection Center
  • H.No: 1-98/13/1, Sai Nagar, Near Hi-Tech Theatre, Madhapur, Hyderabad-500081


    040-48550929

    drlalpathlabsmadhupura@gmail.com

    Collection Center
  • Plot.No. 74, 75, Shirdi Sai Colony, Beeramguda, Ameenpur, Hyderabad, Telangana-502032


    9848095582, 9948354485

    Mallikarjunadiagnostics@gmail.com

    Collection Center
  • 2-177, Near Old Municipal Offices, Behind Gandhi Statue, Main Road, Uppal, Hyderabad, Telangana-500039


    9963005370

    rajulikhutha@gmail.com

    Collection Center