Use of DNA markers for genomic diagnosis of domestic animals: 2. Detection of point mutation causing Hyperkalemic Periodic Paralysis (HYPP) in Quarter horses
DOI:
https://doi.org/10.11606/issn.2318-3659.v33i3p136-139Keywords:
Paralysis, Hyperkalemia, Horses, Equidae, DNA.Abstract
Twelve Quarter horses, descendants from Impressive line, have been analyzed. DNAs, purified from leukocytes of those animals, were submitted to Polymerase Chain Reaction technique (PCR) and digested by Taq I restrictionenzyme. Accordingly the Hyperkalemic Periodic Paralysis (HYPP) genomic diagnosis was established. The tests revealed that 9 animals were carrier heterozygotes (N/H) and 3 normal homozygotes (N/N). Since the development of PCR methodology, it has been possible to diagnose the problem and plan ways to control the spreading of this defective gene in the population, through detection of carrier and normal animals.
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Published
1996-09-01
Issue
Section
BASIC SCIENCES
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The journal content is authorized under the Creative Commons BY-NC-SA license (summary of the license: https://
How to Cite
1.
Garcia JF, Gurgel AS do A, Visintin JA, Lunge VR, Duarte MB, Bertolli JL. Use of DNA markers for genomic diagnosis of domestic animals: 2. Detection of point mutation causing Hyperkalemic Periodic Paralysis (HYPP) in Quarter horses. Braz. J. Vet. Res. Anim. Sci. [Internet]. 1996 Sep. 1 [cited 2025 Feb. 17];33(3):136-9. Available from: https://revistas.usp.br/bjvras/article/view/50181