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A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2

Document Type

Article

Author

Chepurwar, S.; Neef, J.; Strenzke, N.; von Loh, S.M.; Frommolt, P.; Kubisch, C.; Volk, A.E.; Wigger, D.C.; Beutner, D.; Lang-Roth, R.

Source

In: Human Molecular Genetics. (Human Molecular Genetics, 1 April 2023, 32(7):1083-1089)

Subject

Language

English

ISSN

14602083
09646906

Online Access

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

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