Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses-Reference-Cited by-同舟云学术

Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses

Published:2010-03-29 Issue:3 Volume:9 Page:193-207
ISSN:2041-2649
Container-title:Briefings in Functional Genomics
language:en
Short-container-title:Briefings in Functional Genomics

Author:

Bellone R. R.,Forsyth G.,Leeb T.,Archer S.,Sigurdsson S.,Imsland F.,Mauceli E.,Engensteiner M.,Bailey E.,Sandmeyer L.,Grahn B.,Lindblad-Toh K.,Wade C. M.

Publisher

Oxford University Press (OUP)

Subject

Genetics,Molecular Biology,Biochemistry,General Medicine

Link

http://academic.oup.com/bfg/article-pdf/9/3/193/540783/elq002.pdf

Reference44 articles.

1. A missense mutation in the endothelin-B receptor gene is associated with Lethal White Foal Syndrome: an equine version of Hirschsprung Disease

2. A chromosome inversion near the KIT gene and the Tobiano spotting pattern in horses

3. Allelic Heterogeneity at the Equine KIT Locus in Dominant White (W) Horses

4. A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse

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