ATP13A2-related neurodegeneration (PARK9) without evidence of brain iron accumulation

Movement Disorders

Volumn 26, Issue 7, 2011, Pages 1364-1365

  Chien, Hsin Fen ^a   Bonifati, Vincenzo ^b   Barbosa, Egberto Reis ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

^b ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; BRAIN ATROPHY; CASE REPORT; COMPUTER ASSISTED TOMOGRAPHY; GENE MUTATION; HUMAN; LETTER; MISSENSE MUTATION; NEURODEGENERATION WITH BRAIN IRON ACCUMULATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PARKINSONISM; PRIORITY JOURNAL;

BRAIN; HUMANS; IRON; MALE; MUTATION; NERVE DEGENERATION; PROTON-TRANSLOCATING ATPASES;

EID: 79959328761     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.23514     Document Type: Letter

References (2)

1. Schneider SA, Paisan-Ruiz C, Quinn NP. ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation. Mov Disord 2010; 25: 979-984.
2. Di Fonzo A, Chien HF, Socal M. ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease. Neurology 2007; 68: 1557-1562.