Ultrastructural, physiological, and molecular defects in the inner ear of a gene-knockout mouse model for autosomal Alport syndrome

Author:

Cosgrove Dominic,Samuelson Gina,Meehan Daniel T.,Miller Caroline,McGee JoAnn,Walsh Edward J.,Siegel Michel

Publisher

Elsevier BV

Subject

Sensory Systems

Reference43 articles.

1. Deletions in the COL4A5 collagen gene in X-linked Alport syndrome;Antignac;Am. Soc. Clin. Invest.,1994

2. Inner ear and renal diseases;Arnold;Ann. Otol. Rhinol. Laryngol.,1984

3. Atkin, C.L., Gregory, M.C. and Border, W.A. (1988) Alport syndrome. In: Schrier, R.W. and Gottschalk, C.W. (Eds.), Diseases of the Kidney. Little, Brown, Boston, pp. 617–641.

4. Identification of mutations in the COL4A5 collagen gene in Alport syndrome;Barker;Science,1990

5. Burns, W.A. and Bretschnieder, A. (1981) Thin is in: plastic embedding of tissue for light microscopy. Educational Products Division, American Society of Clinical Pathologists, Chicago, IL, pp. 24–25.

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