High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11 gene in patients with Peutz-Jeghers syndrome

BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare hereditary syndrome characterized by the occurrence of hamartomatous polyps in the gastrointestinal tract, mucocutaneous pigmentation and increased risk of cancer in multiple internal organs. Depending on the studied population, its incidence has be...

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Detalhes bibliográficos
Main Authors: Borun, Pawel, Bartkowiak, Anna, Banasiewicz, Tomasz, Nedoszytko, Boguslaw, Nowakowska, Dorota, Teisseyre, Mikolaj, Limon, Janusz, Lubinski, Jan, Kubaszewski, Lukasz, Walkowiak, Jaroslaw, Czkwianianc, Elzbieta, Siolek, Monika, Kedzia, Agnieszka, Krokowicz, Piotr, Cichy, Wojciech, Plawski, Andrzej
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
Assuntos:
Technical Advance
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3681719/
https://ncbi.nlm.nih.gov/pubmed/23718779
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-14-58
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