OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes. (Q36638834)
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scientific article published on 6 January 2016
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes. |
scientific article published on 6 January 2016 |
Statements
OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes (English)
Orly Goldstein
Omri Nayshool
Beatrice Nefussy
Mali Gana-Weisz
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