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

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 CH‐fr...

Descripción completa

Detalles Bibliográficos
Autores principales: Van Poucke, Mario, Van Renterghem, Emilie, Peterson, Mark E., van den Berg, Marit F., Stock, Emmelie, Peelman, Luc J., Daminet, Sylvie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
SMALL ANIMAL
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9511070/
https://www.ncbi.nlm.nih.gov/pubmed/36054182
http://dx.doi.org/10.1111/jvim.16524

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9511070/
https://www.ncbi.nlm.nih.gov/pubmed/36054182
http://dx.doi.org/10.1111/jvim.16524

Ejemplares similares