Truncating SLC12A6 Mutation as a Cause of a Hereditary, Slowly Progressive, Spinocerebellar Ataxia with Severe Central Axonopathy in a Malinois Dog Family

Authors :: Luc Peelman
Emmelie Stock
Laurien Sonck
Leslie Bosseler
Dieter Deforce
Kimberley Stee
Bart J. G. Broeckx
M. Van Poucke
J. Van Dorpe
L. Van Ham
F. Van Nieuwerburgh
Sofie Bhatti
Source :: Journal of Comparative Pathology. 174:181
Publication Year :: 2020
Publisher :: Elsevier BV, 2020.

Subjects :: Genetics
General Veterinary
business.industry
Mutation (genetic algorithm)
Spinocerebellar ataxia
Medicine
business
medicine.disease
Pathology and Forensic Medicine

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