PubMed · 1997 · 89 citations · 41 references
Children with NF1 are susceptible to the development of malignant myeloid disorders both as a primary event and as an SMN. Additional molecular genetic analysis is necessary to determine if the NF1 gene is inactivated by somatic mutation in these secondary leukemias.
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The neurofibromatosis type 1 gene encodes a protein related to GAP
Gangfeng Xu, P. O’Connell, David Viskochil et al. · Cell · 1990 · 1.1K citations
Developmental Biology, Neurogenomics, Neurofibromatosis Type 1 +6