Author:
Kruegel Jenny,Rubel Diana,Gross Oliver
Publisher
Springer Science and Business Media LLC
Reference113 articles.
1. Alport, A. C. Hereditary familial congenital haemorrhagic nephritis. Br. Med. J. 1, 504–506 (1927).
2. Williamson, D. A. Alport's syndrome of hereditary nephritis with deafness. Lancet 2, 1321–1323 (1961).
3. Nagel, M., Nagorka, S. & Gross, O. Novel COL4A5, COL4A4, and COL4A3 mutations in Alport syndrome. Hum. Mutat. 26, 60 (2005).
4. Hertz, J. M., Thomassen, M., Storey, H. & Flinter, F. Clinical utility gene card for: Alport syndrome. Eur. J. Hum. http://dx.doi.org/10.1038/ejhg.2011.237 .
5. Antignac, C. Molecular genetics of basement membranes: the paradigm of Alport syndrome. Kidney Int. Suppl. 49, S29–S33 (1995).
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