Chargement en cours...
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...
Enregistré dans:
| Publié dans: | Audiol Neurootol |
|---|---|
| Auteurs principaux: | , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2015
|
| Sujets: | |
| Accès en ligne: | 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 |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|