Molecular insights into Peutz-Jeghers syndrome: Two probands with a germline mutation of LKB1

Journal of Gastroenterology

Volumn 43, Issue 6, 2008, Pages 492-497

  Hosogi, Hisahiro ^a   Nagayama, Satoshi ^a   Kawamura, Junichiro ^a   Koshiba, Yasushi ^a   Nomura, Akinari ^a   Itami, Atsushi ^a   Okabe, Hiroshi ^a   Satoh, Seiji ^a   Watanabe, Go ^a   Sakai, Yoshiharu ^a  

^a KYOTO UNIVERSITY   (Japan)

Author keywords

Germline mutation; LKB1; Peutz Jeghers syndrome

Indexed keywords

CYCLOOXYGENASE 2; PROTEIN KINASE LKB1;

ADOLESCENT; ADULT; ALLELE; ARTICLE; CASE REPORT; CODON; EXON; FEMALE; GERM LINE; HAMARTOMA; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; INTESTINE INTUSSUSCEPTION; INTESTINE OBSTRUCTION; INTRON; LAPAROSCOPIC SURGERY; MALE; NONSENSE MUTATION; PEUTZ JEGHERS SYNDROME; POLYMERASE CHAIN REACTION; POLYPECTOMY; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN METHYLATION; RNA SPLICING; SEQUENCE ANALYSIS; SKIN PIGMENTATION; SOMATIC MUTATION;

ADOLESCENT; ADULT; CODON, NONSENSE; CYCLOOXYGENASE 2; FEMALE; GERM-LINE MUTATION; HAMARTOMA; HUMANS; INTESTINAL DISEASES; MALE; PEUTZ-JEGHERS SYNDROME; PROTEIN-SERINE-THREONINE KINASES; SEQUENCE ANALYSIS, DNA;

EID: 47349129383     PISSN: 09441174     EISSN: 14355922     Source Type: Journal    
DOI: 10.1007/s00535-008-2185-6     Document Type: Article

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