Author:
Watanabe Atsushi,Takeda Kazuhisa,Ploplis Barbara,Tachibana Masayoshi
Publisher
Springer Science and Business Media LLC
Reference25 articles.
1. Read, A.P. & Newton, V.E. Waardenburg syndrome. J. Med. Genet. 34, 656–665 (1997).
2. Tachibana, M. et al. Ectopic expression of MITF, a gene for Waardenburg syndrome type 2, converts fibroblasts to cells with melanocyte characteristics. Nature Genet. 14, 50–54 (1996).
3. Tachibana, M. et al. Cochlear disorder associated with melanocyte anomaly in mice with a transgenic insertional mutation. Mol. Cell. Neurosci. 3, 433–445 (1992).
4. Tassabehji, M., Newton, V.E. & Read, A.P. Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene. Nature Genet. 8, 251–255 (1994).
5. Nobukuni, Y., Watanabe, A., Takeda, K., Skarka, H. & Tachibana, M. Analyses of loss-of-function mutations of the MITF gene suggest that haploinsufficiency is a cause of Waardenburg syndrome type 2A. Am. J. Hum. Genet. 59, 76–83 (1996).
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