Zhao, Zi-Ye <br/><br/>
A 23-Nucleotide Deletion in STK11 Gene Causes Peutz-Jeghers Syndrome and Malignancy in a Chinese Patient Without a Positive Family History.  [electronic resource] 

 -  Digestive diseases and sciences  11 2017 
 - 3014-3020 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1573-2568 
<br/><br/><label>Standard No.: </label>10.1007/s10620-017-4741-5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>AMP-Activated Protein Kinase Kinases<br/>Adult<br/>Asian People--genetics<br/>Base Sequence<br/>Biomarkers, Tumor--chemistry<br/>China<br/>DNA Mutational Analysis<br/>Exons<br/>Female<br/>Genetic Predisposition to Disease<br/>Heredity<br/>Heterozygote<br/>Humans<br/>Models, Molecular<br/>Pedigree<br/>Peutz-Jeghers Syndrome--diagnosis<br/>Phenotype<br/>Protein Conformation<br/>Protein Serine-Threonine Kinases--chemistry<br/>Sequence Deletion<br/>Structure-Activity Relationship