Genome-wide association and linkage analyses localize a progressive retinal atrophy locus in Persian cats-Reference-Cited by-同舟云学术

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Genome-wide association and linkage analyses localize a progressive retinal atrophy locus in Persian cats

Published:2014-04-29 Issue:7-8 Volume:25 Page:354-362
ISSN:0938-8990
Container-title:Mammalian Genome
language:en
Short-container-title:Mamm Genome

Author:

Alhaddad Hasan,Gandolfi Barbara,Grahn Robert A.,Rah Hyung-Chul,Peterson Carlyn B.,Maggs David J.,Good Kathryn L.,Pedersen Niels C.,Lyons Leslie A.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://link.springer.com/article/10.1007/s00335-014-9517-z/fulltext.html

Reference21 articles.

1. Abecasis GR, Cherny SS, Cookson WO, Cardon LR (2002) Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30:97–101

2. Alloway PG, Howard L, Dolph PJ (2000) The formation of stable rhodopsin-arrestin complexes induces apoptosis and photoreceptor cell degeneration. Neuron 28:129–138

3. Balciuniene J, Johansson K, Sandgren O, Wachtmeister L, Holmgren G, Forsman K (1995) A gene for autosomal dominant progressive cone dystrophy (CORD5) maps to chromosome 17p12-p13. Genomics 30:281–286

4. Camuzat A, Rozet JM, Dollfus H, Gerber S, Perrault I, Weissenbach J, Munnich A, Kaplan J (1996) Evidence of genetic heterogeneity of Leber’s congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13. Hum Genet 97:798–801

5. Filler S, Alhaddad H, Gandolfi B, Kurushima JD, Cortes A, Veit C, Lyons LA, Brem G (2012) Selkirk Rex: morphological and genetic characterization of a new cat breed. J Hered 103:727–733

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