A 23-Nucleotide Deletion in STK11 Gene Causes Peutz-Jeghers Syndrome and Malignancy in a Chinese Patient Without a Positive Family History. [electronic resource]
Producer: 20171106Description: 3014-3020 p. digitalISSN:- 1573-2568
- AMP-Activated Protein Kinase Kinases
- Adult
- Asian People -- genetics
- Base Sequence
- Biomarkers, Tumor -- chemistry
- China
- DNA Mutational Analysis
- Exons
- Female
- Genetic Predisposition to Disease
- Heredity
- Heterozygote
- Humans
- Models, Molecular
- Pedigree
- Peutz-Jeghers Syndrome -- diagnosis
- Phenotype
- Protein Conformation
- Protein Serine-Threonine Kinases -- chemistry
- Sequence Deletion
- Structure-Activity Relationship
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Publication Type: Case Reports; Journal Article
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