Shared burden of ultra-rare genetic variants across a spectrum of motor neuron diseases.

Transl Neurodegener · 2025 · PMC12570777 · PMID 41152957

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marginally significantno p-value reported

Interestingly, AP4S1 was marginally significant in the burden test of ProjectMinE and significant in the meta-analysis ( P = 0.017, Table S3h).

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