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[These data suggest that a (UV-) mutated PTCH gene is important for sporadic BCC formation independent of clinical phenotype and that the IVS16-80G/C and/or IVS17+21G/A SNP site might be important for tumorigenesis in certain BCC patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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