Výsledky vyhľadávania - "restriction fragment length polymorphism SHM"

Combining MYD88 L265P mutation detection and clonality determination on CSF cellular and cell‐free DNA improves diagnosis of primary CNS lymphoma Autor Bravetti, Clotilde, Degaud, Michaël, Armand, Marine, Sourdeau, Elise, Mokhtari, Karima, Maloum, Karim, Osman, Jennifer, Verrier, Patricia, Houillier, Caroline, Roos‐Weil, Damien, Soussain, Carole, Choquet, Sylvain, Hoang‐Xuan, Khe, Le Garff‐Tavernier, Magali, Denis, Jérôme Alexandre, Davi, Frédéric

“…Summary Diagnosis of primary central nervous system lymphoma (PCNSL) is challenging, and although brain biopsy remains the gold standard, cerebrospinal fluid…”
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