Publication | Open Access
ASAH1 variant causing a mild SMA phenotype with no myoclonic epilepsy: a clinical, biochemical and molecular study
23
Citations
15
References
2016
Year
Clinical DisordersMendelian DisorderNeurological DisorderAsah1 VariantGenetic DisorderPathologyMyoclonic EpilepsyMild Sma PhenotypeNeuroscienceNeurologyNeuropathologyMedicineMolecular Medicine
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