Novel mutations in one allele in a Chinese family with neurofibromatosis type 1: Including a complex insertion-deletion mutation. [electronic resource]
- The Journal of dermatology Nov 2016
- 1332-1335 p. digital
Publication Type: Case Reports; Journal Article
1346-8138
10.1111/1346-8138.13498 doi
Adult DNA Mutational Analysis Female Genes, Neurofibromatosis 1 Humans INDEL Mutation Infant Male Neurofibromatosis 1--genetics