A novel <it>de novo </it>mutation in the serine-threonine kinase <it>STK11 </it>gene in a Korean patient with Peutz-Jeghers syndrome
<p>Abstract</p> <p>Background</p> <p>Peutz-Jeghers syndrome (PJS) is an unusual autosomal dominant disorder characterized by mucocutaneous pigmentation and multiple gastrointestinal hamartomatous polyps. Patients with PJS are at an increased risk of developing multi-org...
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Main Authors: | , , , , , , , |
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Format: | Book |
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BMC,
2008-05-01T00:00:00Z.
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