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RT @NeuroGen_papers: PubMed: OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes. https://t.c…
RT @NeuroGen_papers: PubMed: OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes. https://t.c…
PubMed: OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes. https://t.co/4npORknaCF
OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes. https://t.co/bq038EnC9i
OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes https://t.co/fvU67Rv7jC