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Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11

Document Type

Article

Author

Reinson, Karit; Kovacs-Nagy, Reka; Õiglane-Shlik, Eve; Pajusalu, Sander; Nõukas, Margit; Wintjes, Liesbeth T.; van den Brandt, Frans C.A.; Brink, Maaike; Acker, Till; Ahting, Uwe; Hahn, Andreas; Schänzer, Anne; Haack, Tobias B.; Rodenburg, Richard J.; Õunap, Katrin

Source

In European Journal of Medical Genetics November 2019 62(11)

Subject

Language

ISSN

1769-7212

Online Access

Full Text (ScienceDirect 종량제) Full Text (Clinical Key) Web of Science JCR 저널정보 Scopus Find it@PNU

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