Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I.
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| Description | scientific article |
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author: Mary Reilly Eleonore Fröhlich Andreas Janecke Michaela Auer-Grumbach |
| Publication date | December 30, 2010 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |