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Prevention of Auditory Dysfunction in Hypothyroid Tshr Mutant Mice by Thyroxin Treatment During Development

Based on previous work, it is clear that genetically hypothyroid Tshrhyt mutant mice are congenitally deaf [O'Malley et al. (1995) Hear. Res. 88: 181-189, Sprinkle et al. 2001b, J. Assoc. Res. Otolaryngol. DOI: 10.1007/s101620010077]. However, the extent to which auditory development is depende...

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Detalhes bibliográficos
Main Authors: Sprenkle, Pamela M., McGee, JoAnn, Bertoni, John M., Walsh, Edward J.
Formato: Artigo
Idioma:Inglês
Publicado em: Springer-Verlag 2001
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3201071/
https://ncbi.nlm.nih.gov/pubmed/11833608
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s101620010078
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