Low-burden TP53 mutations represent frequent genetic events in CLL with an increased risk for treatment initiation

Laszlo, T (author)

Kotmayer, L (author)

Fesus, V (author)

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Hegyi, L (author)

Grof, S (author)

Nagy, A (author)

Kajtar, B (author)

Balogh, A (author)

Weisinger, J (author)

Masszi, T (author)

Nagy, Z (author)

Farkas, P (author)

Demeter, J (author)

Istenes, I (author)

Sazsz, R (author)

Gergely, L (author)

Sulak, A (author)

Borbenyi, Z (author)

Levai, D (author)

Schneider, T (author)

Pettendi, P (author)

Bodai, E (author)

Szerafin, L (author)

Rejto, L (author)

Batai, A (author)

Domotor, MA (author)

Santa, H (author)

Plander, M (author)

Szendrei, T (author)

Hamed, A (author)

Lazar, Z (author)

Pauker, Z (author)

Radvanyi, G (author)

Kiss, A (author)

Korosmezey, G (author)

Jakucs, J (author)

Dombi, PJ (author)

Simon, Z (author)

Klucsik, Z (author)

Gurzo, M (author)

Tiboly, M (author)

Vidra, T (author)

Ilonczai, P (author)

Bors, A (author)

Andrikovics, H (author)

Egyed, M (author)

Szekely, T (author)

Masszi, A (author)

Alpar, D (author)

Matolcsy, A (author)

Karolinska Institutet

Bodor, C (author)

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 (creator_code:org_t)

2024

2024

English.

In: The journal of pathology. Clinical research. - 2056-4538. ; 10:1, s. e351-

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• Journal article (peer-reviewed)