A unified process for neurological disease

Science

Volumn 343, Issue 6170, 2014, Pages 497-498

  Singleton, Andrew B ^a  

^a NATIONAL INSTITUTE ON AGING   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DISEASE INCIDENCE; GENETIC ANALYSIS; MUTATION; NEUROLOGY; PATHOGENICITY;

ALZHEIMER DISEASE; BIOINFORMATICS; GENE MUTATION; GENETIC ANALYSIS; HEREDITARY MOTOR SENSORY NEUROPATHY; MOLECULAR PATHOLOGY; MUTATION; NEUROLOGIC DISEASE; PARKINSON DISEASE; PATHOGENESIS; PATHOGENICITY; PRIORITY JOURNAL; PYRAMIDAL TRACT; SHORT SURVEY; ANIMAL; EXOME; GENETIC ASSOCIATION; GENETICS; HUMAN; METABOLISM; MOTOR NEURON DISEASE; NERVE CELL; NOTE;

ANIMALS; EXOME; GENETIC ASSOCIATION STUDIES; HUMANS; MOTOR NEURON DISEASE; NEURONS; PYRAMIDAL TRACTS; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 84893049118     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1250172     Document Type: Short Survey

References (4)

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3. J. K. Fink, Acta Neuropathol. 126, 307 (2013).
4. E. C. Oates et al., Am. J. Hum. Genet. 92, 965 (2013).