Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng0999_113.pdf
Reference30 articles.
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3. Kumar, S., Marres, H.A.M., Cremers, C.W.R.J. & Kimberling, W.J. Identification of three novel mutations in human EYA1 protein associated with branchio-oto-renal syndrome. Hum. Mutat. 11, 443–449 (1998).
4. Vincent, C. et al. BOR and BO syndromes are allelic defects of EYA1. Eur. J. Hum. Genet. 5, 242–246 (1997).
5. Durbec, P. et al. GDNF signalling through the Ret receptor tyrosine kinase. Nature 381, 789–793 (1996).
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