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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...
Autores principales: | Thakur, Nikita, Reddy, D Nageshwar, Rao, G Venkat, Mohankrishna, P, Singh, Lalji, Chandak, Giriraj R |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2006
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Materias: | |
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 |
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