Close and regular surveillance is key to prevent severe complications for Peutz-Jeghers syndrome patients without gastrointestinal polyps: case report of a novel STK11 mutation (c.471_472delCT) in a Chinese girl

[1] Giardiello FM(2000)Very high risk of cancer in familial Peutz-Jeghers syndrome Gastroenterology 119 1447-1453

[2] Brensinger JD(2010)Peutz-Jeghers syndrome: a systematic review and recommendations for management Gut 59 975-986

[3] Tersmette AC(2007)Germline mutation in the STK11 gene in a girl with an ovarian Sertoli cell tumour Eur J Pediatr 166 1083-1085

[4] Goodman SN(2011)High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome Gut 60 141-147

[5] Petersen GM(2017)Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient BMC Med Genet 18 130-W258

[6] Booker SV(2014)SWISS-MODEL: modelling protein tertiary and quaternary structure using evolutionary information Nucleic Acids Res 42 W252-415

[7] Cruz-Correa M(2006)Peutz-Jeghers syndrome and management recommendations Clin Gastroenterol Hepatol 4 408-90

[8] Offerhaus JA(1997)Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis Nat Genet 15 87-3465

[9] Beggs AD(2010)Germline mutation analysis of STK11 gene using direct sequencing and multiplex ligation-dependent probe amplification assay in Korean children with Peutz-Jeghers syndrome Dig Dis Sci 55 3458-52

[10] Latchford AR(1988)The protein kinase family: conserved features and deduced phylogeny of the catalytic domains Science 241 42-5114

[1] Giardiello FM(2000)Very high risk of cancer in familial Peutz-Jeghers syndrome Gastroenterology 119 1447-1453

[2] Brensinger JD(2010)Peutz-Jeghers syndrome: a systematic review and recommendations for management Gut 59 975-986

[3] Tersmette AC(2007)Germline mutation in the STK11 gene in a girl with an ovarian Sertoli cell tumour Eur J Pediatr 166 1083-1085

[4] Goodman SN(2011)High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome Gut 60 141-147

[5] Petersen GM(2017)Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient BMC Med Genet 18 130-W258

[6] Booker SV(2014)SWISS-MODEL: modelling protein tertiary and quaternary structure using evolutionary information Nucleic Acids Res 42 W252-415

[7] Cruz-Correa M(2006)Peutz-Jeghers syndrome and management recommendations Clin Gastroenterol Hepatol 4 408-90

[8] Offerhaus JA(1997)Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis Nat Genet 15 87-3465

[9] Beggs AD(2010)Germline mutation analysis of STK11 gene using direct sequencing and multiplex ligation-dependent probe amplification assay in Korean children with Peutz-Jeghers syndrome Dig Dis Sci 55 3458-52

[10] Latchford AR(1988)The protein kinase family: conserved features and deduced phylogeny of the catalytic domains Science 241 42-5114