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Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome

Document Type

Article

Author

Nesbit, M.A.; Bowl, M.R.; Harding, B.; Ali, A.; Thakker, R.V.; Ayala, A.; Crowe, C.; Dobbie, A.; Hampson, G.; Holdaway, I.; Levine, M.A.; McWilliams, R.; Rigden, S.; Sampson, J.; Williams, A.J.

Source

In: Journal of Biological Chemistry. (Journal of Biological Chemistry, 21 May 2004, 279(21):22624-22634)

Subject

Language

English

ISSN

00219258

Online Access

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

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