Identification of Gene Mutations in Primary Pediatric Cardiomyopathy by Whole Exome Sequencing

• Main Authors: Kitiwan Rojnueangnit, Boonchu Sirichongkolthong, Ratthapon Wongwandee, Thanitchet Khetkham, Saisuda Noojarern, Arthaporn Khongkraparn, Duangrurdee Wattanasirichaigoon
• Other Authors: Thammasat University Hospital
• Format: Article
• Published: 2020
• Subjects: Medicine
• Online Access: https://repository.li.mahidol.ac.th/handle/123456789/52337
• Institution: Mahidol University

© 2019, Springer Science+Business Media, LLC, part of Springer Nature. Pediatric primary cardiomyopathy is rare but serious, having high mortality; hypertrophic and dilated types are the most common. Its etiology has been mainly considered idiopathic; however, next generation sequencing techniques h...