Human Genome Epidemiology Literature Finder
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Query Trace: Neurodegenerative Diseases and C19orf12[original query] |
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Mutational analysis of the CYP7B1, PNPLA6 and C19orf12 genes in autosomal recessive hereditary spastic paraplegia. Molecular and cellular probes 2015 Dec . Schubert Sarah F, Hoffjan Sabine, Dekomien Gabrie |
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