共 50 条
- [44] Analysis of 200 unrelated individuals with a constitutional NF1 deep intronic pathogenic variant reveals that variants flanking the alternatively spliced NF1 exon 31 [23a] cause a classical neurofibromatosis type 1 phenotype while altering predominantly NF1 isoform type II HUMAN GENETICS, 2023, 142 (07) : 849 - 861
- [45] A somatic splice-site variant in PIK3R1 in a patient with vascular overgrowth and low immunoglobulin levels: A case report MOLECULAR GENETICS & GENOMIC MEDICINE, 2023,
- [47] Immunotherapy with pembrolizumab in a patient with advanced non-small-cell lung cancer with high PD-L1 expression and MET exon 14 splice site mutation ONCOLOGY IN CLINICAL PRACTICE, 2023, 19 (01): : 63 - 68