Publication | Open Access

Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1

Neuro-oncologyHnpcc-associated TumoursSomatic VariantGenetic DisorderPathologyNeurofibromatosis Type 1NeurologyNeuropathologyMedicineEarly-onset Haematological Malignancy