Found: 3
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OPA1 mutations induce mitochondrial DNA instability and optic atrophy plus phenotypes.
- Published in:
- Brain: A Journal of Neurology, 2008, v. 131, n. 2, p. 338, doi. 10.1093/brain/awm298
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- Publication type:
- Article
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 10, p. 1893, doi. 10.1093/hmg/ddr071
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- Publication type:
- Article
Soluble urokinase-type plasminogen activator receptor (suPAR) as an independent factor predicting worse prognosis and extra-bone marrow involvement in multiple myeloma patients.
- Published in:
- British Journal of Haematology, 2003, v. 120, n. 6, p. 953, doi. 10.1046/j.1365-2141.2003.04176.x
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- Publication type:
- Article