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ReviewNeurogenetics2021

SPG43 and ALS-like syndrome in the same family due to compound heterozygous mutations of the C19orf12 gene: a case description and brief review.

Gauthier Remiche et al.PubMed ↗Publisher ↗

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3 papers cite it

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Full record →Abstract, authors, funding and every citing paper · PMID 33394258