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Mutations in Bcl9 and Pygo genes cause congenital heart defects by tissue-specific perturbation of Wnt/β-catenin signaling

Document Type

Article

Author

Cantù, C.; Felker, A.; Zimmerli, D.; Prummel, K.D.; Cabello, E.M.; Chiavacci, E.; Kirchgeorg, L.; Burger, S.; Valenta, T.; Hausmann, G.; Burger, A.; Basler, K.; Mosimann, C.; Méndez-Acevedo, K.M.; Panáková, D.; Ripoll, J.; Vilain, N.; Aguet, M.

Source

In: Genes and Development. (Genes and Development, 1 November 2018, 32(21-22):1443-1458)

Subject

Language

English

ISSN

15495477
08909369

Online Access

Full Text (ECC - 개별구독 전자저널) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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