A novel de novo mutation in the serine-threonine kinase STK11 gene in a Korean patient with Peutz-Jeghers syndrome

BMC Medical Genetics

Volumn 9, Issue , 2008, Pages

  Yoo, Jong Ha ^a   Yoo, Jee Hyoung ^a   Choi, Yoon Jung ^a   Kang, Jung Gu ^a   Sun, Young Kyu ^a   Ki, Chang Seok ^b   Lee, Kyung A ^c   Choi, Jong Rak ^c  

^a National Health Insurance Corporation   (South Korea)

^b Sungkyunkwan University School of Medicine   (South Korea)

^c Yonsei University College of Medicine   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; EXONUCLEASE; EXONUCLEASE IX; EXONUCLEASE VI; GUANINE; PROTEIN KINASE LKB1; PROTEIN SERINE THREONINE KINASE; STK11 PROTEIN, HUMAN;

ADOLESCENT; ARTICLE; BASE PAIRING; CARBOXY TERMINAL SEQUENCE; CASE REPORT; CONTROLLED STUDY; DNA FLANKING REGION; EXON; GENE DELETION; GENE LOSS; GENE SEQUENCE; GENETIC IDENTIFICATION; GERM LINE; HUMAN; INTRON; KOREA; MALE; MUTATIONAL ANALYSIS; PEUTZ JEGHERS SYNDROME; STOP CODON; DNA SEQUENCE; FEMALE; GENETICS; MUTATION; PATHOLOGY; PEDIGREE; POLYMERASE CHAIN REACTION;

ADOLESCENT; FEMALE; HUMANS; MALE; MUTATION; PEDIGREE; PEUTZ-JEGHERS SYNDROME; POLYMERASE CHAIN REACTION; PROTEIN-SERINE-THREONINE KINASES; SEQUENCE ANALYSIS, DNA;

EID: 45549095515     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-9-44     Document Type: Article

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