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Prevalence of the mutation in cyclophilin B (PPIB), a causal candidate gene for HERDA, among Quarter Horses in France.

Vet. Dermatol.2011 Apr;22(2):206-8. doi:10.1111/j.1365-3164.2010.00941.x. Epub 2010 Nov 30
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摘要


Hereditary equine regional dermal asthenia in Quarter Horses is an inherited degenerative skin disease. Initially reported as hyperelastosis cutis, has a phenotype of hyperextensible, fragile skin, with secondary seromas, haematomas, ulcers and scarring. It primarily affects the dorsal aspect of the body. An autosomal recessive mode of inheritance is considered likely, with affected horses more at risk to produce affected offspring. A mutation in cyclophilin B (PPIB) as a novel, causal candidate gene for HEduanyu1650 has been described, and verified as segregating with carriers and affected horses. Screening of control Quarter Horses in the USA has indicated a 3.5% carrier frequency. The prevalence of this mutation among Quarter Horses in France was determined to be 1.6%.

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