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Figure 2 | Journal of Medical Case Reports

Figure 2

From: Gliomatosis cerebri type II: two case reports

Figure 2

(a) Sequence around codon 248 of TP53 showing the mutated base which determines an arginine to tryptophan substitution. (b) The PTEN point mutation at the intron 2 splice donor site causes a defective splicing which likely results in a non-functional protein.

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