Mosaicism of activating FGFR3 mutations in human skin causes epidermal nevi
J. Clin. Invest. 116:8 doi:10.1172/JCI28163
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Figure 2
FGFR3 gene.

The position of the mutations covered by the SNaPshot multiplex assay is indicated. Codons are numbered according to the FGFR3 IIIb isoform; potential mutations of the stop codon 809 in exon 19 associated with TD I were analyzed by direct sequencing. C, C-terminus; Ig I, Ig II, Ig III, Ig-like domains I–III; N, N-terminus; TM, transmembrane domain; TKI, TKII, tyrosine kinase domains I–II.