Noonan Syndrome Confirmed toKRASGene Mutation: A Case ofKRASGene Mutation
Author:
Affiliation:
1. Department of Pediatrics, CHA Gangnam Medical Center, CHA University, Seoul, Korea.
Publisher
The Korean Society of Neonatology
Link
http://neo-med.org/upload/pdf/J Korean Soc Neonatol._18_2_374_378.pdf
Reference20 articles.
1. Noonan Syndrome
2. Noonan syndrome and clinically related disorders
3. PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype–phenotype correlation in Korean patients with Noonan syndrome
4. Noonan syndrome: A review
5. Genetic heterogeneity in Noonan syndrome: Evidence for an autosomal recessive form
Cited by 1 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. An atypical case of Noonan syndrome with KRAS mutation diagnosed by targeted exome sequencing;Annals of Pediatric Endocrinology & Metabolism;2017-09-30
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