Clinical spectrum of disease associated with ATP1A3 mutations

The Lancet Neurology

Volumn 11, Issue 9, 2012, Pages 741-743

  Ozelius, Laurie J ^a  

^a MOUNT SINAI SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; ATP1A3 PROTEIN; UNCLASSIFIED DRUG;

ALTERNATING HEMIPLEGIA OF CHILDHOOD; CHILDHOOD DISEASE; DISEASE ASSOCIATION; DYSTONIA; ENVIRONMENTAL STRESS; EXOME; GENE; GENE EXPRESSION; HEMIPLEGIA; HETEROZYGOTE; HUMAN; LETTER; MISSENSE MUTATION; PARKINSONISM; PHENOTYPE; PRIORITY JOURNAL;

EXOME; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HEMIPLEGIA; HUMANS; MALE; MUTATION; SODIUM-POTASSIUM-EXCHANGING ATPASE;

EID: 84865133147     PISSN: 14744422     EISSN: 14744465     Source Type: Journal    
DOI: 10.1016/S1474-4422(12)70185-0     Document Type: Letter

References (10)

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