Must Peutz-Jeghers syndrome patients have the LKB1/STK11 gene mutation? A case report and review of the literature
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DOI: 10.12998/wjcc.v6.i8.224
Abstract: Peutz-Jeghers syndrome (PJS) is an autosomal dominant inherited disease, which is characterized by mucocutaneous pigmentation and multiple gastrointestinal hamartoma polyps. The germline mutation of LKB1/STK11 gene on chromosome 19p13.3 is considered to be the hereditary… read more here.
Keywords: stk11 gene; lkb1 stk11; gene mutation; gene ... See more keywords