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Publikováno v:
Revista de gastroenterologia de Mexico (English). 85(2)
Peutz-Jeghers syndrome is a rare autosomal dominant inherited disease caused by a germline mutation of the STK11/LKB1 gene, located on chromosome 19p13.3. It is characterized by mucocutaneous hyperpigmentation, hamartomatous polyposis, and predisposi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6231d512c1811d2ece884cf51146671d
https://pubmed.ncbi.nlm.nih.gov/31257110
https://pubmed.ncbi.nlm.nih.gov/31257110
