Complete STK11 Deletion and Atypical Symptoms in Peutz-Jeghers Syndrome-Reference-Cited by-同舟云学术

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Complete STK11 Deletion and Atypical Symptoms in Peutz-Jeghers Syndrome

Published:2017-09-01 Issue:5 Volume:37 Page:462-464
ISSN:2234-3806
Container-title:Annals of Laboratory Medicine
language:en
Short-container-title:Ann Lab Med

Author:

Jang Myeong Sun¹,Lee Yoo Min¹,Ko Bong Min²,Kang Goeun³,Kim Jong-Won⁴,Hong Yong Hee¹

Affiliation:

1. Department of Pediatrics and Digestive Disease Center and Research Institute, Soonchunhyang University College of Medicine, Bucheon, Korea

2. Department of Internal Medicine, Soonchunhyang University College of Medicine, Bucheon, Korea

3. Department of Laboratory Medicine, Mokpo Hankook Hospital, Mokpo, Korea

4. Department of Laboratory Medicine and Clinical Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea

Funder

Soonchunhyang University

Publisher

Annals of Laboratory Medicine

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Link

https://synapse.koreamed.org/pdf/10.3343/alm.2017.37.5.462

Reference8 articles.

1. A serine/threonine kinase gene defective in Peutz–Jeghers syndrome

2. Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis

3. Growth suppression by Lkb1 is mediated by a G1 cell cycle arrest

4. Complete germline deletion of the STK11 gene in a family with Peutz–Jeghers syndrome

5. Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. STK11 Causative Variants and Copy Number Variations Identified in Thai Patients With Peutz-Jeghers Syndrome;Cureus;2023-02-01

2. Delayed diagnosis of Peutz–Jeghers syndrome due to pathological information loss or mistake in family/personal history;Orphanet Journal of Rare Diseases;2021-06-08

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