Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation.

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Published in Hum Mol Genet on July 01, 1996

Authors

M X Guan1, N Fischel-Ghodsian, G Attardi

Author Affiliations

1: Division of Biology, California Institute of Technology, Pasadena 91125, USA.

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