Identification of Gene Mutations in Primary Pediatric Cardiomyopathy by Whole Exome Sequencing
© 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...
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Main Authors: | Kitiwan Rojnueangnit, Boonchu Sirichongkolthong, Ratthapon Wongwandee, Thanitchet Khetkham, Saisuda Noojarern, Arthaporn Khongkraparn, Duangrurdee Wattanasirichaigoon |
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Other Authors: | Thammasat University Hospital |
Format: | Article |
Published: |
2020
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Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/52337 |
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Institution: | Mahidol University |
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