Publication | Closed Access
A novel SCN1A mutation associated with severe GEFS+ in a large South American pedigree
40
Citations
26
References
2005
Year
Novel Scn1a MutationMendelian DisorderGenetic DisorderMedicineGeneticsPathologyMolecular GeneticsDisease Gene IdentificationMolecular DiagnosticsSevere Gefs+Variant Interpretation
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