| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson’s disease risk in Taiwan
|
Fonzo, Alessio Di
|
|
2006
|
7 |
3 |
p. 133-138
|
artikel
|
| 2 |
Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer’s disease in Mexican families
|
Yescas, Petra
|
|
2006
|
7 |
3 |
p. 195-200
|
artikel
|
| 3 |
Investigation of autism and GABA receptor subunit genes in multiple ethnic groups
|
Collins, Ann L.
|
|
2006
|
7 |
3 |
p. 167-174
|
artikel
|
| 4 |
Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL
|
Annunen-Rasila, Johanna
|
|
2006
|
7 |
3 |
p. 185-194
|
artikel
|
| 5 |
Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene
|
Okamoto, Yuji
|
|
2006
|
7 |
3 |
p. 175-183
|
artikel
|
| 6 |
Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysis
|
Lin, Ping-I
|
|
2006
|
7 |
3 |
p. 157-165
|
artikel
|
| 7 |
Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity
|
Stevanin, Giovanni
|
|
2006
|
7 |
3 |
p. 149-156
|
artikel
|
| 8 |
Transcriptome analysis reveals link between proteasomal and mitochondrial pathways in Parkinson’s disease
|
Duke, D. C.
|
|
2006
|
7 |
3 |
p. 139-148
|
artikel
|
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