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Case report: A rare variant m.4135T>C in the MT-ND1 gene leads to Leber hereditary optic neuropathy and altered respiratory chain supercomplexes

Document Type

Article

Author

Rákosníková, T.; Kelifová, S.; Štufková, H.; Lokvencová, K.; Honzík, T.; Hansíková, H.; Tesařová, M.; Lišková, P.; Kousal, B.; Martínek, V.

Source

In: Frontiers in Genetics. (Frontiers in Genetics, 2023, 14)

Subject

Language

English

ISSN

16648021

Online Access

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

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