We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitlePrevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairmentAuthorsHutchin, T.P.; Thompson, K.R.; Parker, M.; Newton, V.; Bitner-Glindzicz, M.; Mueller, R.F.PublicationJournal of Medical Genetics (JMG), 2001, Vol 38, Issue 4, p229ISSN0022-2593Publication typearticle