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Stk11 gene - PowerPoint PPT Presentation

Peutz-Jeghers Syndrome

Peutz-Jeghers Syndrome . Chad Manning. Background. Autosomal dominant 1/25000 affected worldwide 70% familial cases 50% sporadic cases mutated in the STK11 gene 16p13.3 encoding for serine/threonine kinase 11 Relationship is unknown. Clinical Features.

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Stk11 gene - PowerPoint PPT Presentation

Peutz-Jeghers Syndrome