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A mutation in CABP2, expressed in cochlear hair cells, causes autosomal-recessive hearing impairment

Document Type

Article

Author

Schrauwen, I.; Sommen, M.; Claes, C.; Fransen, E.; Van Camp, G.; Helfmann, S.; Predoehl, F.; Picher, M.M.; Moser, T.; Inagaki, A.; Lee, A.; Tabatabaiefar, M.A.; Chaleshtori, M.H.; Seco, C.Z.; Oostrik, J.; Kremer, H.; Dheedene, A.; Coucke, P.

Source

In: American Journal of Human Genetics. (American Journal of Human Genetics, 5 October 2012, 91(4):636-645)

Subject

Language

English

ISSN

00029297
15376605

Online Access

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

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