MSH2, MSH6, MLH1, and PMS2 Immunohistochemistry As Highly Sensitive Screening Method for DNA Mismatch Repair Deficiency Syndromes in Pediatric High-Grade Glioma. Lea L. Friker , Thomas Perwein , Andreas Waha , Evelyn Dörner , Rebecca Klein , Mirjam Blattner-Johnson , Julian P. Layer , Dominik Sturm , Gunther Nussbaumer , Robert Kwiecien , Isabel Spier , Stefan Aretz , Kornelius Kerl , Ulrike Hennewig , Marius Rohde , Axel Karow , Ingmar Bluemcke , Ann Kristin Schmitz , Harald Reinhard , Pablo Hernáiz Driever , Susanne Wendt , Annette Weiser , Ana S. Guerreiro Stücklin , Nicolas U. Gerber , André O. von Bueren , Claudia Khurana , Norbert Jorch , Maria Wiese , Christian P. Kratz , Matthias Eyrich , Michael Karremann , Ulrich Herrlinger , Michael Hölzel , David T. W. Jones , Marion Hoffmann , Torsten Pietsch , Gerrit H. Gielen , Christof M. Kramm Acta Neuropathologica（2025）
Key words
Pediatric high-grade glioma, Lynch syndrome, Constitutional mismatch repair deficiency, Immunohistochemistry
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