Auditory dysfunction in type 2 Stickler Syndrome

PURPOSE: To present the extent and site of lesion of auditory dysfunction in a large cohort of individuals with type 2 Stickler Syndrome. Type 2 Stickler Syndrome results from a mutation in the gene coding for α-1 type XI pro-collagen, which has been identified in the human vitreous, cartilage and t...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Eur Arch Otorhinolaryngol
Päätekijät: Alexander, Philip, Gomersall, Philip, Stancel-Lewis, Jack, Fincham, Gregory Scott, Poulson, Arabella, Richards, Allan, McNinch, Annie, Baguley, David M., Snead, Martin
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Springer Berlin Heidelberg 2020
Aiheet:
Otology
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC8165062/
https://ncbi.nlm.nih.gov/pubmed/32901364
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00405-020-06306-y
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