Clinical and Genetic Study of Children With Peutz-Jeghers Syndrome Identifies a High Frequency of STK11 De Novo Mutation
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DOI: 10.1097/mpg.0000000000002166
Abstract: Objectives: The present study aims to identify the genotype-phenotype correlation in children with Peutz-Jeghers Syndrome (PJS) through the analysis of STK11 gene mutations in the context of clinical and pathological characteristics. Method: In this observational… read more here.
Keywords: peutz jeghers; high frequency; children peutz; study ... See more keywords