De novo germline mutation in the serine–threonine kinase STK11/LKB1 gene associated with Peutz–Jeghers syndrome.
Hernan, I.; Rolg, I.; Martin, B.; Gamundi, M.J.; Martinez-Gimeno, M.; Carballo, M.; Clinical Genetics, 2004, vol. 66, issue 1, p 58, ISSN 00099163. ISBN 00099163.

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