A novel missense mutation of the STK11 gene in a Chinese family with Peutz-Jeghers syndrome

Overview of attention for article published in BMC Gastroenterology, December 2022

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https://t.co/PKrLRb7TTg　 Peutz-Jeghers症候群家系においてSTK11遺伝子のエクソン4における新規ヘテロ接合型バリアント（c.521A > C）を認めた中国からの報告です。

📌STK11 gene, phenotype expansion #GastrointestinalDisease #Cancer #BirthDefect #raredisease A novel missense mutation of the STK11 gene in a Chinese family with Peutz-Jeghers syndrome https://t.co/YN9XdJeCiA

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