Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa-Reference-Cited by-同舟云学术

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Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa

Published:2000-11 Issue:3 Volume:26 Page:270-271
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Gal Andreas,Li Yun,Thompson Debra A.,Weir Jessica,Orth Ulrike,Jacobson Samuel G.,Apfelstedt-Sylla Eckart,Vollrath Douglas

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1100_270.pdf

Reference15 articles.

1. D'Cruz, P.M. et al. Hum. Mol. Genet. 9, 645–652 (2000).

2. Bourne, M.C., Campbell, D.A. & Tansley, K. Br. J. Ophthalmol. 22, 613–622 (1938).

3. Bourne, M.C. & Gruneberg, H. J. Hered. 30, 130–136 (1939).

4. Mullen, R.J. & LaVail, M.M. Science 192, 799–801 (1976).

5. Dowling, J.E. & Sidman, R.L. J. Cell Biol. 14, 73–109 (1962).

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