STK11 gene analysis reveals a significant number of splice mutations in Chinese PJS patients
Author:
Funder
National Natural Science Foundation of China
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference49 articles.
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1. Genetic variation at a splicing branch point in intron 7 of STK11: a rare variant decreasing its expression in a Chinese family with Peutz–Jeghers syndrome;World Journal of Surgical Oncology;2024-07-30
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3. Changes of gut microbiota and short chain fatty acids in patients with Peutz–Jeghers syndrome;BMC Microbiology;2023-11-30
4. Peutz-Jeghers syndrome without STK11 mutation may correlate with less severe clinical manifestations in Chinese patients;World Journal of Gastroenterology;2023-06-07
5. Genotype-phenotypic correlation of Peutz-Jeghers syndrome on the example of a series of clinical cases;Koloproktologia;2022-06-21
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