Mutation characteristic of STK11 gene in Chinese with Peutz-Jeghers syndrome

Chinese Journal of Medical Genetics

Volumn 18, Issue 1, 2001, Pages 4-7

  Li, Y ^a   Lu, X ^a   Xia, J ^a   Tang, X ^a   Xia, K ^a   He, Y ^a   Zhang, G ^a  

^a CENTRAL SOUTH UNIVERSITY   (China)

Author keywords

DNA sequencing; Gene mutation; Peutz Jeghers syndrome; STK11 gene

Indexed keywords

ARTICLE; CHINESE; DISEASE ASSOCIATION; DNA SEQUENCE; GENE MUTATION; GENETIC ANALYSIS; HUMAN; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PEUTZ JEGHERS SYNDROME; SEQUENCE ANALYSIS;

EXONS; GERM-LINE MUTATION; HUMANS; PEUTZ-JEGHERS SYNDROME; POLYMERASE CHAIN REACTION; PROTEIN-SERINE-THREONINE KINASES;

EID: 0035117308     PISSN: 10039406     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (7)

1. Locatigation of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis
2. Peutz-Jeghers syndrome caused by mutation in a novel serine threonine kinase
3. A serine/threonine kinase gene defectne in Peutz-Jeghers syndrome
4. 11 gene mutation in Chinese with PJS
5. Peutz-Jeghers syndrome: Most, but not all, families are compatible with linkage to 19p 13.3
6. 1 germline mutations are not identified in most Peutz-Jeghers syndrome patients