A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients

BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare multi-organ cancer syndrome and understanding its genetic basis may help comprehend the molecular mechanism of familial cancer. A number of germ line mutations in the STK11 gene, encoding a serine threonine kinase have been reported in these patient...

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Detalles Bibliográficos
Autores principales: Thakur, Nikita, Reddy, D Nageshwar, Rao, G Venkat, Mohankrishna, P, Singh, Lalji, Chandak, Giriraj R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1609100/
https://www.ncbi.nlm.nih.gov/pubmed/17010210
http://dx.doi.org/10.1186/1471-2350-7-73

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1609100/
https://www.ncbi.nlm.nih.gov/pubmed/17010210
http://dx.doi.org/10.1186/1471-2350-7-73

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