Cite
HARVARD Citation
Hutchin, T. et al. (2001). Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairment. Journal of medical genetics. 38 (4), pp. 229-231. [Online].
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Hutchin, T. et al. (2001). Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairment. Journal of medical genetics. 38 (4), pp. 229-231. [Online].