Detection of Mutations in Genes Associated with Hearing Loss Using a Microarray-Based Approach

Knowing the etiology of hearing loss in a person has implications for counseling and management of the condition. More than 50% of cases of early onset, nonsyndromic sensorineural hearing loss are attributable to genetic factors. However, deafness is a genetically heterogeneous condition and it is t...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Siemering, Kirby, Manji, Shehnaaz S.M., Hutchison, Wendy M., Du Sart, Desiree, Phelan, Dean, Dahl, Hans-Henrik M.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Society for Investigative Pathology 2006
Gaiak:
Regular Articles
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1867613/
https://ncbi.nlm.nih.gov/pubmed/16931589
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/jmoldx.2006.050147
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