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. 2017 May 5;6(4):247–251. doi: 10.1055/s-0037-1602816

Fig. 4.

Fig. 4

( A ) A heterozygous c.1115G > A [p.(Cys372Tyr)] missense mutation (arrow) was detected in the patient in FGFR1 exon 10 near the predicted transmembrane domain that was not detected in normal controls. ( B ) An FGFR1 monomer is shown with the predicted location of the Y372C mutation adjacent to the transmembrane domain.