Apparent high prevalence of mitochondrial DNA mutations in congenital/childhood non-syndromic sensorineural hearing impairment

Hutchin, T., Thompson, K., Parker, M., Newton, V., Van Camp, G., Bitner-Glindzicz, M., & Mueller, R. (2000). Apparent high prevalence of mitochondrial DNA mutations in congenital/childhood non-syndromic sensorineural hearing impairment. Journal of Medical Genetics : an international peer-reviewed journal for health professionals and researchers in all areas of genetics, 37, S21-S21. https://doi.org/10.1136/jmg.37.9.692 (Original work published 2000)