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

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