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The genetics of Aicardi-Goutières syndrome.
Crow YJ
Eur J Paediatr Neurol. 2002;6 Suppl A:A33-5; discussion A37-9, A77-86.
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Adolescent; Child; Child, Preschool; Chromosome Mapping; Consanguinity; Disease Progression; Humans; Infant; Infant, Newborn; Lod Score; Phenotype; Syndrome; cerebrospinal fluid: Cerebrospinal Fluid Proteins; cerebrospinal fluid: Interferon-alpha; diagnosis: Basal Ganglia Diseases; diagnosis: Calcinosis; diagnosis: Hereditary Central Nervous System Demyelinating Diseases; diagnosis: Lymphocytosis; genetics: Genetic Markers