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A Genetic Triple Play: Adolescent-onset Hyperkinetic Syndrome with Multilocus KMT2B and FGF14 Variants and Familial Hunter Syndrome in One Pedigree

Genetic Variants in Acetylcholine Processing and Significant Improvement with Pyridostigmine in a Patient with Postural Orthostatic Tachycardia Syndrome.

Geographic and Ethnic Variation in Migraine Diagnosis and Treatment Among Asian Subgroups in the United States: A National Electronic Health Record Study