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Patients and providers should treat them as directional rather than definitive, and decisions about participating in trials or accessing investigational therapies should always involve a specialist in endocrinology or metabolic medicine.

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinsons disease

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Saneto, RP, Cohen, BH, Copeland, WC, Naviaux, RK 2013, Alpers-Huttenlocher Syndrome, Pediatric Neurology , vol