Identification of a Novel Twinkle Mutation in a Family With Infantile Onset Spinocerebellar Ataxia by Whole Exome Sequencing (Q59698178)
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- Identification of a novel Twinkle mutation in a family with infantile onset spinocerebellar ataxia by whole exome sequencing
| Language | Label | Description | Also known as |
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| English | Identification of a Novel Twinkle Mutation in a Family With Infantile Onset Spinocerebellar Ataxia by Whole Exome Sequencing |
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Statements
Identification of a Novel Twinkle Mutation in a Family With Infantile Onset Spinocerebellar Ataxia by Whole Exome Sequencing (English)
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Identification of a novel Twinkle mutation in a family with infantile onset spinocerebellar ataxia by whole exome sequencing (English)
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March 2012
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46
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3
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172-177
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172-7
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