• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Thr155Asn (c.464C>A); ClinVar=VCV000406564; Zygosity=Unspecified (PubMed=18487078).
  

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PubMed=18487078; DOI=10.1016/j.oraloncology.2008.02.006
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