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Gustavson syndrome is caused by an in-frame deletion in RBMX associated with potentially disturbed SH3 domain interactions

Document Type

Article

Author

Johansson, J.; Lidéus, S.; Frykholm, C.; Gudmundsson, S.; Ekvall, S.; Molin, A.-M.; Pham, M.; Ameur, A.; Annerén, G.; Wilbe, M.; Bondeson, M.-L.; Gunnarsson, C.; Mihalic, F.; Jemth, P.; Vihinen, M.; Lagerstedt-Robinson, K.; Nordgren, A.

Source

In: European Journal of Human Genetics. (European Journal of Human Genetics, March 2024, 32(3):333-341)

Subject

Language

English

ISSN

14765438
10184813

Online Access

Web of Science JCR 저널정보 Scopus Find it@PNU

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