Exome sequencing sheds light on hereditary spastic paraplegia

Nature Reviews Neurology

Volumn 10, Issue 3, 2014, Pages 124-

  Chase, Alex ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ALZHEIMER DISEASE; AMYOTROPHIC LATERAL SCLEROSIS; EPILEPSY; EXOME; GENE MUTATION; GENE SEQUENCE; GENOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; NONHUMAN; NOTE; PARKINSON DISEASE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN INTERACTION; ANIMAL; GENETIC ASSOCIATION; GENETICS; METABOLISM; MOTOR NEURON DISEASE; NERVE CELL; PYRAMIDAL TRACT;

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

EID: 84895927741     PISSN: 17594758     EISSN: 17594766     Source Type: Journal    
DOI: 10.1038/nrneurol.2014.27     Document Type: Note

References (1)

1. Novarino, G. et al. Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders. Science 343, 506-511 (2014