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Sammanfattning

The present invention relates to methods for detecting a genetic deletion at the SHOX locus of a horse, where the presence of such a genetic deletion indicates that the horse is a carrier of disease-causing mutation that can lead to skeletal atavism. The invention further provides nucleic acid primers and probes for use in methods for detecting the presence or absence of disease-causing genetic deletion at the SHOX locus of a horse.

SLU författare

UKÄ forskningsämne

Klinisk vetenskap

More information

Assignees: Sofia MIKKO, Leif Andersson, Gabriella LINDGREN, Carl-Johan RUBIN, Bhanu CHOWDHARY, Terje RAUDSEPP, Evan E. EICHLER, John Huddleston, Maika MALIG

Permanent länk till denna sida (URI)

https://res.slu.se/id/publ/99858