Utilization of mouse models in the discovery of human disease genes
Author:
Publisher
Elsevier BV
Subject
Drug Discovery,Pharmacology
Reference40 articles.
1. A recurrent deletion in the KIT (mast/stem cell growth factor receptor) proto-oncogene is a frequent cause of human piebaldism
2. Insight into the microphthalmia gene
3. Defective myosin VIIA gene responsible for Usher syndrome type IB
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