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An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1

Document Type

Article

Author

Yu, H.-C.; Scharer, G.; Quintana, A.M.; Coughlin II, C.R.; Geiger, E.A.; Schneck, U.; Van Hove, J.L.K.; Shaikh, T.H.; Sloan, J.L.; Achilly, N.P.; Manoli, I.; Venditti, C.P.; Brebner, A.; Watkins, D.; Rosenblatt, D.S.; Suormala, T.; Fowler, B.; Baumgartner, M.R.

Source

In: American Journal of Human Genetics. (American Journal of Human Genetics, 5 September 2013, 93(3):506-514)

Subject

Language

English

ISSN

00029297
15376605

Online Access

Full Text (ScienceDirect 종량제) Full Text (ScienceDirect O/A) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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