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This page is a summary of: Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient, BMC Medical Genetics, November 2017, Springer Science + Business Media,
DOI: 10.1186/s12881-017-0471-y.
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