OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes.
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| Description | scientific article published on 6 January 2016 |
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author: Alan Renton Avi Orr-Urtreger Bryan Traynor |
| Publication date | January 6, 2016 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |