Mutations in LKB1 lead to Peutz-Jeghers syndrome (PJS). However, only a subset of PJS patients harbours LKB1 mutations. We performed a mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADalpha, and MO25alpha, in 28 LKB1-negative PJS patients. No disease-causing mutations were detected in the studied genes in PJS patients from different European populations
Peutz-Jeghers syndrome (PJS) is an autosomal dominantly inherited disease characterized by hamartoma...
Peutz-Jeghers syndrome (PJS) is an autosomal dominantly inherited disease characterized by multiple ...
Abstract Background Germline mutations or large-scale deletions in the coding region and splice site...
Peutz-Jeghers syndrome (PJS) is an autosomal dominant disease characterized by mucocutaneous pigment...
BACKGROUND: LKB1/STK11 germline mutations cause Peutz-Jeghers syndrome (PJS). The existence of a sec...
Peutz-Jeghers syndrome (PJS) is a rare autosomal dominantly inherited disorder with variable express...
Pathogenic mutations in the serine/threonine kinase STK11 (alias LKB1) cause Peutz-Jeghers syndrome ...
Germline mutations of the tumor suppressor gene LKB1/STK11 are responsible for the Peutz-Jeghers syn...
Germline mutations of the tumor suppressor gene LKB1/STK11 are responsible for the Peutz-Jeghers syn...
Germline mutations of the tumor suppressor gene LKB1/STK11 are responsible for the Peutz-Jeghers syn...
Germline mutations of the LKB1 gene are associated with Peutz-Jeghers syndrome (PJS), which is chara...
Germline mutations of the LKB1 (STK11) serine/threonine kinase gene (chromosome 19p13.3) cause Peutz...
BACKGROUND: Germline mutations or large-scale deletions in the coding region and splice sites of STK...
Germline mutations in the LKB1/STK11 tumour suppressor gene cause Peutz-Jeghers syndrome (PJS), a ra...
Background. Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant inherited disease caused by a ...
Peutz-Jeghers syndrome (PJS) is an autosomal dominantly inherited disease characterized by hamartoma...
Peutz-Jeghers syndrome (PJS) is an autosomal dominantly inherited disease characterized by multiple ...
Abstract Background Germline mutations or large-scale deletions in the coding region and splice site...
Peutz-Jeghers syndrome (PJS) is an autosomal dominant disease characterized by mucocutaneous pigment...
BACKGROUND: LKB1/STK11 germline mutations cause Peutz-Jeghers syndrome (PJS). The existence of a sec...
Peutz-Jeghers syndrome (PJS) is a rare autosomal dominantly inherited disorder with variable express...
Pathogenic mutations in the serine/threonine kinase STK11 (alias LKB1) cause Peutz-Jeghers syndrome ...
Germline mutations of the tumor suppressor gene LKB1/STK11 are responsible for the Peutz-Jeghers syn...
Germline mutations of the tumor suppressor gene LKB1/STK11 are responsible for the Peutz-Jeghers syn...
Germline mutations of the tumor suppressor gene LKB1/STK11 are responsible for the Peutz-Jeghers syn...
Germline mutations of the LKB1 gene are associated with Peutz-Jeghers syndrome (PJS), which is chara...
Germline mutations of the LKB1 (STK11) serine/threonine kinase gene (chromosome 19p13.3) cause Peutz...
BACKGROUND: Germline mutations or large-scale deletions in the coding region and splice sites of STK...
Germline mutations in the LKB1/STK11 tumour suppressor gene cause Peutz-Jeghers syndrome (PJS), a ra...
Background. Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant inherited disease caused by a ...
Peutz-Jeghers syndrome (PJS) is an autosomal dominantly inherited disease characterized by hamartoma...
Peutz-Jeghers syndrome (PJS) is an autosomal dominantly inherited disease characterized by multiple ...
Abstract Background Germline mutations or large-scale deletions in the coding region and splice site...