Enter your terms above and click the 'Search' button.

Showing articles 0 to 3 of 3 Filter Applied: gene mutation (Click to remove) Clinicopathologic Conference,Aceruloplasminemia, Hereditary NEJM 383:1974-1983, Case 35-2020, 2020 A 27-Year Old Man with Rapidly Progressive Coma Neurol 85:e74-e78, Wong,J.M.,et al, 2015 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 Showing articles 0 to 3 of 3