Clinical and Molecular Phenotype of Aicardi-Goutières SyndromeGillian Rice, Rasieka Jayatunga, Teresa Patrick et al.|The American Journal of Human Genetics|2007Cited by 449
Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesisMichèl A.A.P. Willemsen, Ron A. Wevers, Alec Aeby et al.|Brain|2010Cited by 233