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Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.

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Asymmetric assembly of congested contiguous stereocenters via photobiocatalytic three-component radical coupling.

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[Invasive interventions for asymptomatic stenotic internal carotid artery lesions in paradigm of modern optimal drug therapy].

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Benign intracranial hypertension induced by deficiency of vitamin A during infancy

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