Neuroferritinopathy in a French family with late onset dominant dystonia.

Journal of medical genetics

Volumn 40, Issue 5, 2003, Pages

  Chinnery, P F ^a   Curtis, A R ^a   Fey, C ^a   Coulthard, A ^a   Crompton, D ^a   Curtis, A ^a   Lombes A ^a   Burn, J ^a  

^a NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

IRON;

ADULT; ARTICLE; CORPUS STRIATUM; DOMINANT GENE; DYSTONIA; EXTRAPYRAMIDAL SYNDROME; FRANCE; GENETICS; HAPLOTYPE; HUMAN; METABOLISM; MIDDLE AGED; ONSET AGE; PATHOLOGY; PATHOPHYSIOLOGY; UNITED KINGDOM;

ADULT; AGE OF ONSET; BASAL GANGLIA DISEASES; CORPUS STRIATUM; DYSTONIA; ENGLAND; FRANCE; GENES, DOMINANT; HAPLOTYPES; HUMANS; IRON; MIDDLE AGED;

MLCS; MLOWN;

EID: 0043280850     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.40.5.e69     Document Type: Article

References (0)