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Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON)

Document Type

Article

Author

Peron, C.; Mauceri, R.; Cabassi, T.; Segnali, A.; Tiranti, V.; Maresca, A.; Carelli, V.; Iannielli, A.; Broccoli, V.; Rizzo, A.; Sciacca, F.L.

Source

In: Stem Cell Research. (Stem Cell Research, October 2020, 48)

Subject

Language

English

ISSN

18767753
18735061

Online Access

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

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