Association of recessive c.430G>A (p.(Gly144Arg)) thyroid peroxidase variant with primary congenital hypothyroidism in cats

Abstract Background Primary congenital hypothyroidism (CH) is a rare endocrine disorder in cats with a largely unknown genetic cause. Objectives Describe the clinical presentation of CH in 11 affected cats and identify the causal genetic variant. Animals Eleven CH‐cats from 10 unrelated families, 11...

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Bibliographic Details
Main Authors: Mario Van Poucke, Emilie Van Renterghem, Mark E. Peterson, Marit F. van denBerg, Emmelie Stock, Luc J. Peelman, Sylvie Daminet
Format: Article
Language:English
Published: Wiley 2022-09-01
Series:Journal of Veterinary Internal Medicine
Subjects:
Online Access:https://doi.org/10.1111/jvim.16524