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A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients.
Thakur N, Reddy DN, Rao GV, Mohankrishna P, Singh L, Chandak GR
BMC Med Genet 2006, 7:73
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Research article    
A novel de novo mutation in the serine-threonine kinase STK11 gene in a Korean patient with Peutz-Jeghers syndrome
Yoo JH, Yoo JH, Choi YJ, Kang JG, Sun YK, Ki CS, Lee KA, Choi JR
BMC Medical Genetics 2008, 9:44 (22 May 2008)
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