Novel homozygous OPA3 mutation in an Afghani family with 3-methylglutaconic aciduria type III and optic atrophy.
| Autor: | Gaier, Eric D.1,2,3,4 (AUTHOR), Sahai, Inderneel3,5 (AUTHOR), Wiggs, Janey L.2,3 (AUTHOR), McGeeney, Brian3,6 (AUTHOR), Hoffman, Jodi7,8 (AUTHOR), Peeler, Crandall E.7,9,10 (AUTHOR) Crandall.Peeler@bmc.org |
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| Zdroj: | Ophthalmic Genetics. Dec2019, Vol. 40 Issue 6, p570-573. 4p. |
| Databáze: | Academic Search Ultimate |
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