Research Article
A Novel MLH1 Initiation Codon Mutation (c.3G>T) in a Large Chinese Lynch Syndrome Family with Different Onset Age and mRNA Expression Level
Figure 3
(a) and (b) Sanger sequencing of MLH1 (c.3G>T, p.Met1Ile) in these family members identified in the proband and his father (GenBank Accession: NM_000249.3).
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