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Gene identification in the congenital disorders of glycosylation type i by whole-exome sequencing

Document Type

Article

Author

Timal, S.; Lefeber, D.J.; Huijben, K.; Rodenburg, R.J.; Eidhof, I.; Van den heuvel, L.; Wevers, R.A.; Hoischen, A.; Gilissen, C.; Veltman, J.; Morava, E.; Lehle, L.; Adamowicz, M.; Sykut-cegielska, J.; Paprocka, J.; Jamroz, E.; Van spronsen, F.J.; Körner, C.; Thiel, C.

Source

In: Human Molecular Genetics. (Human Molecular Genetics, October 2012, 21(19):4151-4161)

Subject

Language

English

ISSN

09646906
14602083

Online Access

Full Text (Oxford University Press) Full Text (OUP Near Archive) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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