Exome sequencing identifies a missense mutation in Isl1 associated with low penetrance otitis media in dearisch mice

BACKGROUND: Inflammation of the middle ear (otitis media) is very common and can lead to serious complications if not resolved. Genetic studies suggest an inherited component, but few of the genes that contribute to this condition are known. Mouse mutants have contributed significantly to the identi...

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Detalhes bibliográficos
Main Authors: Hilton, Jennifer M, Lewis, Morag A, Grati, M'hamed, Ingham, Neil, Pearson, Selina, Laskowski, Roman A, Adams, David J, Steel, Karen P
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2011
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3308053/
https://ncbi.nlm.nih.gov/pubmed/21936904
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gb-2011-12-9-r90
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