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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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| Publicado no: | Audiol Neurootol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| 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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