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Mutations in the ABCC8 gene are also associated with an autosomal dominant form of type 2 diabetes and with an autosomal recessive disorder termed hyperinsulinemic hypoglycemia of infancy

Otolaryngol Head Neck Surg 148(5):827833 Semedo MG, Dias-Silva N, Miguis J, Pita JR (2021) Quinine in otology and neurotology: ototoxicity and historic role in therapy

The WHO ICD-10 uses a single, general code (G20) , which is simpler to apply but does not allow documentation of motor complications such as dyskinesia or off episodesimportant factors for tracking disease progression

Review No Abstract [18] Lu, S.C

The supplement industry is far less regulated than pharmaceuticals, and product quality varies enormously