Parkinsonism in GTP cyclohydrolase 1 mutation carriers

Brain

Volumn 138, Issue 5, 2015, Pages e349-

  Guella, Ilaria ^a   Sherman, Holly E ^a   Appel Cresswell, Silke ^b   Rajput, Alex ^c   Rajput, Ali H ^c   Farrer, Matthew J ^a  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^b UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^c SASKATOON HEALTH REGION   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA SYNUCLEIN; DOPAMINE; GUANOSINE TRIPHOSPHATE CYCLOHYDROLASE I; LEVODOPA;

DIFFUSE LEWY BODY DISEASE; DOPA RESPONSIVE DYSTONIA; DOPAMINE METABOLISM; EXOME; GENE FREQUENCY; GENE SEQUENCE; GENERALIZED DYSTONIA; GENETIC CODE; GENETIC DISORDER; GENETIC VARIABILITY; HETEROZYGOTE; HUMAN; IMMUNOHISTOCHEMISTRY; LETTER; LEWY BODY; LOSS OF FUNCTION MUTATION; MISSENSE MUTATION; NEUROFIBRILLARY TANGLE; ONSET AGE; PARKINSON DISEASE; PARKINSONISM; PATHOGENICITY; PRIORITY JOURNAL; PROGRESSIVE SUPRANUCLEAR PALSY; SHY DRAGER SYNDROME; STRIATONIGRAL DEGENERATION; FEMALE; GENETICS; MALE; MUTATION;

FEMALE; GTP CYCLOHYDROLASE; HETEROZYGOTE; HUMANS; MALE; MUTATION; PARKINSON DISEASE;

EID: 84929658359     PISSN: 00068950     EISSN: 14602156     Source Type: Journal    
DOI: 10.1093/brain/awu341     Document Type: Letter

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