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Familial cardiac septal defect due to a novel nine‐base deletion in TBX20

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Bibliographic Details
Published in:	Pediatrics international 2022-01, Vol.64 (1), p.e14995-n/a
Main Authors:	Yamamoto, Hidenori, Inagaki, Hidehito, Hayano, Satoshi, Kurahashi, Hiroki, Kato, Taichi
Format:	Article
Language:	English
Subjects:	cardiac septal defect congenital heart disease deletion Gene deletion Heart Septal Defects Heart Septal Defects, Atrial - diagnosis Heart Septal Defects, Atrial - genetics Humans Mutation Pediatrics T-Box Domain Proteins - genetics TBX20 whole exome sequencing
Citations:	Items that this one cites
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