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

Document Type

Artikel

Author

Johansson, J; Lideus, S; Frykholm, C; Gunnarsson, C; Mihalic, F; Gudmundsson, S; Ekvall, S; Molin, AM; Pham, M; Vihinen, M; Lagerstedt-Robinson, K; Nordgren, A; Jemth, P; Ameur, A; Anneren, G; Wilbe, M; Bondeson, ML

Source

European journal of human genetics : EJHG. 32(3):333-341

Subject

Medicin och hälsovetenskap

Language

English
English

ISSN

1476-5438

Online Access

Open Access (SwePub) Web of Science JCR 저널정보 Find it@PNU

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