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Histopathology of the Human Inner Ear in Alström Syndrome

Alström syndrome is an autosomal recessive syndromic genetic disorder caused by mutations in the ALMS1 gene. Sensorineural hearing loss occurs in greater than 85% of patients. Histopathology of the inner ear abnormalities in the human has not previously been fully described. Histopathology of the in...

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Detalhes bibliográficos
Publicado no:Audiol Neurootol
Main Authors: Nadol, Joseph B., Marshall, Jan D., Bronson, Roderick T.
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4540704/
https://ncbi.nlm.nih.gov/pubmed/26111748
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000381935
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