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    MPL W515/S505 MUTATION ANALYSIS, (FOR SUSPECTED CASES OF POLYCYTHEMIA VERA WHERE JAK 2 V617F IS NEGATIVE) FOR CONFIRMATION OF PV.

    Identifies hotspot MPL mutations critical for myeloproliferative disease diagnosis and management.

    Chhusya Bahal (Chhusya Galli), Jyatha, Thamel, Kathmandu 44600, Bagmati
    Instant Confirmation
    Verified
    Description
    🩺 MPL W515/S505 Mutation Analysis at MedEx Neo Clinic, Kathmandu 📍 The MPL W515/S505 mutation analysis at MedEx Neo Clinic, Kathmandu focuses on detecting specific hotspot mutations (W515 and S505) in the MPL gene, which are strongly associated with myeloproliferative disorders including essential thrombocythemia and primary myelofibrosis. These mutations cause constitutive activation of the thrombopoietin receptor, leading to abnormal blood cell production. This molecular test uses targeted PCR and sequencing techniques for accurate mutation identification, aiding precise diagnosis and targeted treatment strategies.
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    MPL W515/S505 MUTATION ANALYSIS, (FOR SUSPECTED CASES OF POLYCYTHEMIA VERA WHERE JAK 2 V617F IS NEGATIVE) FOR CONFIRMATION OF PV.

    18,000 NPR