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
Research output: Contribution to journal › Journal article › Research › peer-review
Original language | English |
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Journal | Hum. Genet. |
Issue number | vol. 109 |
Pages (from-to) | 498-502 |
Publication status | Published - 2001 |
ID: 142057