Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairment

Genetic factors are the major causes of childhood hearing impairment. Whereas autosomal recessive mutations account for the majority of prelingual non-syndromic sensorineural hearing impairment (NSSHI), the relative contribution of mitochondrial DNA (mtDNA) mutations to childhood onset NSSHI has not...

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Bibliografische gegevens
Hoofdauteurs: Hutchin, T, Thompson, K, Parker, M, Newton, V, Bitner-Glindzicz, M, Mueller, R
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BMJ Group 2001
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Original Articles
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1734848/
https://ncbi.nlm.nih.gov/pubmed/11283203
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.38.4.229
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