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Filter Applied: hemiparesis,transient (Click to remove)

Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study
Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012

Metabolic Disease and Stroke: MELAS
emedicine.com, Mandava,P.,et al, 2006



Showing articles 0 to 2 of 2