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Type III 3-Methylglutaconic Aciduria (Optic Atrophy Plus Syndrome, or Costeff Optic Atrophy Syndrome): Identification of the OPA3 Gene and Its Founder Mutation in Iraqi Jews |
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| Authors: | Yair Anikster Robert Kleta Avraham Shaag William A. Gahl Orly Elpeleg |
| Affiliation: | Section on Human Biochemical Genetics, Heritable Disorders Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA. |
| Abstract: | |
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