Mutations in S-cone pigment genes and the absence of colour vision in two species of nocturnal primate-Reference-Cited by-同舟云学术

Mutations in S-cone pigment genes and the absence of colour vision in two species of nocturnal primate

Published:1996-06-22 Issue:1371 Volume:263 Page:705-710
ISSN:0962-8452
Container-title:Proceedings of the Royal Society of London. Series B: Biological Sciences
language:en
Short-container-title:Proc. R. Soc. Lond. B

Author:

Publisher

The Royal Society

Subject

General Agricultural and Biological Sciences,General Environmental Science,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

https://royalsocietypublishing.org/doi/pdf/10.1098/rspb.1996.0105

Reference32 articles.

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3. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

4. Multiple human D5 dopamine receptor genes: a functional receptor and two pseudogenes.

5. Humphries P. Kenna P. & Farrar G. J. 1994 Autosomal dominant retinitis pigmentosa. In Molecular genetics of inherited eye disorders (ed. A. F. Wright & B. Jay) pp. 153-172. Reading: Harwood Academic Publishers.

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