OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes

Overview of attention for article published in Neurology, January 2016

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OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes.

Alzforum, 15 Jan 2016

Goldstein O, Nayshool O, Nefussy B, Traynor BJ, Renton AE, Gana-Weisz M, Drory VE, Orr-Urtreger A.

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