Startle disease in Irish wolfhounds associated with a microdeletion in the glycine transporter GlyT2 gene
Author:
Funder
Medical Research Council
Publisher
Elsevier BV
Subject
Neurology
Reference27 articles.
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3. Identification of the microdeletion breakpoint in a GLRA1 null allele of Turkish hyperekplexia patients;Becker;Hum. Mutat.,2006
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