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A hypomorphic variant of choroideremia is associated with a novel intronic mutation that leads to exon skipping

Document Type

Article

Author

Waldock, W.J.; Taylor, L.J.; Sperring, S.; Martinez-Fernandez de la Camara, C.; Yusuf, I.H.; MacLaren, R.E.; Staurenghi, F.; Whitfield, J.; Clouston, P.

Source

In: Ophthalmic Genetics. (Ophthalmic Genetics, 2024, 45(2):210-217)

Subject

Language

English

ISSN

17445094
13816810

Online Access

Full Text (T&F Medical) Web of Science JCR 저널정보 Scopus Find it@PNU

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