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SynthesisNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2026

A novel homozygous variant in the POLR1A gene: a complicated hereditary spastic paraplegia (c-HSP) or a hypomyelinating leukodystrophy type-27 (HLD27) phenotype?

Masoud Tajamolian et al.PubMed ↗Publisher ↗

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Full record →Abstract, authors, funding and every citing paper · PMID 42271096