scholarly article | Q13442814 |
P356 | DOI | 10.1212/WNL.56.6.802 |
P698 | PubMed publication ID | 11274324 |
P50 | author | Filippo Maria Santorelli | Q60541206 |
P2093 | author name string | G Casari | |
D Fortini | |||
F Pierelli | |||
V Bonifati | |||
R Carrozzo | |||
G Meco | |||
C Casali | |||
N Vanacore | |||
G D'Amati | |||
G Fabbrini | |||
N Locuratolo | |||
M Damiano | |||
A Patrignani | |||
A Pierallini | |||
G A Amabile | |||
P433 | issue | 6 | |
P921 | main subject | Parkinson's disease | Q11085 |
parkinsonian syndrome | Q1531991 | ||
mitochondrial myopathy | Q6881881 | ||
P1104 | number of pages | 4 | |
P304 | page(s) | 802-805 | |
P577 | publication date | 2001-03-01 | |
P1433 | published in | Neurology | Q1161692 |
P1476 | title | Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family | |
P478 | volume | 56 |
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