A child with juvenile myelomonocytic leukemia possessing a concurrent germline CBL mutation and a NF1 variant of uncertain significance: A rare case with a common problem in the era of high-throughput sequencing

Publication date: Available online 12 September 2020Source: Journal of the Formosan Medical AssociationAuthor(s): Wei-Hao Wang, Meng-Yao Lu, Cheng-Hong Tsai, Shih-Chung Wang, Shu-Wei Chou, Shiann-Tarng Jou
Source: Journal of the Formosan Medical Association - Category: General Medicine Source Type: research