Loss of function in ROBO1 is associated with tetralogy of Fallot and septal defects
BACKGROUND: Congenital heart disease (CHD) is a common birth defect affecting approximately 1% of newborns. Great progress has been made in elucidating the genetic aetiology of CHD with advances in genomic technology, which we leveraged in recovering a new pathway affecting heart development in huma...
Κύριοι συγγραφείς: | Kruszka, P, Tanpaiboon, P, Neas, K, Crosby, K, Berger, S, Martinez, A, Addissie, Y, Pongprot, Y, Sittiwangkul, R, Silvilairat, S, Makonkawkeyoon, K, Yu, L, Wynn, J, Bennett, J, Mefford, H, Reynolds, W, Liu, X, Mommersteeg, M, Chung, W, Lo, C, Muenke, M |
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Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
BMJ Publishing Group
2017
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