Clinical and Genetic Analyses of 38 Chinese Patients with Peutz-Jeghers Syndrome.

Conclusion: This study expanded the spectrum of STK11 gene mutations and further elucidated individuals with null mutations of STK11 typically had an earlier onset of PJS symptoms and needed earlier management. PMID: 32462036 [PubMed - in process]

https://www.ncbi.nlm.nih.gov/pubmed/32462036?dopt=Abstract

Source: Biomed Res - May 30, 2020 Category: Research Authors: Wu BD, Wang YJ, Fan LL, Huang H, Zhou P, Yang M, Shi XL Tags: Biomed Res Int Source Type: research