No abstract available
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Aging, Premature / genetics
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DNA Mutational Analysis
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Exons
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Genetic Testing / methods
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Genotype
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Hearing Loss, Sensorineural / genetics
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Humans
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Membrane Proteins / genetics
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Mitochondrial Diseases / genetics
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Mutation
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Optic Atrophy / genetics
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Pathology, Molecular
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Risk Assessment
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Sensitivity and Specificity
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Wolfram Syndrome / diagnosis*
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Wolfram Syndrome / epidemiology
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Wolfram Syndrome / genetics*
Substances
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CISD2 protein, human
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Membrane Proteins
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wolframin protein