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Human Genetics
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December 6, 2001
A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect
D L Thiselton, C Alexander, A Morris, et al.
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Showing results (11-20 of 11) with videos related to
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This site can display upto 11 results.
Human Genetics
|
December 6, 2001
A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect
D L Thiselton, C Alexander, A Morris, et al.
Page
of 2