| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype
|
Pirkevi, C.
|
|
2009
|
10 |
3 |
p. 271-273
|
artikel
|
| 2 |
A new complex homozygous large rearrangement of the PINK1 gene in a Sudanese family with early onset Parkinson’s disease
|
Cazeneuve, Cécile
|
|
2009
|
10 |
3 |
p. 265-270
|
artikel
|
| 3 |
Association between migraine and a functional polymorphism at the dopamine β-hydroxylase locus
|
Fernandez, F.
|
|
2009
|
10 |
3 |
p. 199-208
|
artikel
|
| 4 |
Examination of association of genes in the serotonin system to autism
|
Anderson, B. M.
|
|
2009
|
10 |
3 |
p. 209-216
|
artikel
|
| 5 |
Extended tracts of homozygosity identify novel candidate genes associated with late-onset Alzheimer’s disease
|
Nalls, M. A.
|
|
2009
|
10 |
3 |
p. 183-190
|
artikel
|
| 6 |
Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred
|
Cuenca-León, Ester
|
|
2008
|
10 |
3 |
p. 191-198
|
artikel
|
| 7 |
Interaction of the SPG21 protein ACP33/maspardin with the aldehyde dehydrogenase ALDH16A1
|
Hanna, Michael C.
|
|
2009
|
10 |
3 |
p. 217-228
|
artikel
|
| 8 |
Molecular analysis of NPC1 and NPC2 gene in 34 Niemann–Pick C Italian Patients: identification and structural modeling of novel mutations
|
Fancello, Tatiana
|
|
2009
|
10 |
3 |
p. 229-239
|
artikel
|
| 9 |
Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes
|
Russo, S.
|
|
2009
|
10 |
3 |
p. 241-250
|
artikel
|
| 10 |
The spectrum of somatic and germline NF1 mutations in NF1 patients with spinal neurofibromas
|
Upadhyaya, Meena
|
|
2009
|
10 |
3 |
p. 251-263
|
artikel
|
| 11 |
Whole-genome conditional two-locus analysis identifies novel candidate genes for late-onset Parkinson’s disease
|
González-Pérez, A.
|
|
2009
|
10 |
3 |
p. 173-181
|
artikel
|
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