Signs and symptoms
Genes
Methods
Disclaimer
About us
Publications
Contact us
Patients
Users
Database
Login
Overview of included studies for PARK-SNCA:
Click here for summary of patients' characteristics
Click here for summary of genetic findings
Click here to show world map of all countries
Filter for
all included patients
index patients only
AAO < 50 (adjustable)
AAO >= 50 (adjustable)
females only
males only
homozygous only
heterozygous only
compound heterozygous only
homozygous and compound heterozygous
carrying
definitely pathogenic mutations
probably pathogenic mutations
possibly pathogenic mutations
c.(?_-1471)_(575_?)dup
c.(?_-1471)_(575_?)tri
c.464C>A
c.136G>A
c.150G>A
c.150T>G
c.152G>A
c.157G>A
c.158C>A
c.88G>C
Country
Argentina
Bolivia
China
Finland
France
Germany
Greece
Italy
Japan
Pakistan
Poland
South Korea
Spain
Sweden
United Kingdom
United States
Study
Study design
N cases
Ethnicities
Sex
(%
♂
)
Mean AAO (+/- SD)
Reported mutations
Nuytemans, 2009
Mutational screen
1
n.a.
n.a.
68
c.(?_-1471)_(*575_?)dup
: het
Ibáñez, 2009
Other/Mixed
5
n.a.
20%
44(+/-6)
c.(?_-1471)_(*575_?)dup
: het
c.(?_-1471)_(*575_?)tri
: het
Troiano, 2008
Case report/Case series
1
n.a.
0%
35
c.(?_-1471)_(*575_?)dup
: het
Uchiyama, 2008
Other/Mixed
2
A
50%
60(+/-18)
c.(?_-1471)_(*575_?)dup
: het
Ikeuchi, 2008
Family study
4
A
75%
50(+/-20)
c.(?_-1471)_(*575_?)dup
: hom
c.(?_-1471)_(*575_?)dup
: het
Markopoulou, 2008
Family study
8
C
63%
50(+/-10)
p.Ala53Thr
: het
Ahn, 2008
Other/Mixed
3
A
67%
52(+/-13)
c.(?_-1471)_(*575_?)dup
: het
Ki, 2007
Family study
1
A
100%
35
p.Ala53Thr
: het
Fuchs, 2007
Family study
2
C
100%
51(+/-28)
c.(?_-1471)_(*575_?)dup
: het
c.(?_-1471)_(*575_?)tri
: het
Nishioka, 2006
Other/Mixed
3
A
67%
44(+/-6)
c.(?_-1471)_(*575_?)dup
: het
« First page
‹ Previous
1
2
3
4
5
6
Next ›
Last page »
Show all studies on one page
© University of Lübeck. Last updated on
Dec. 2, 2020. Version: 3.5.95
MDSGene works best with JavaScript enabled. Please follow
these instructions
to activate JavaScript in your web browser.
MDSGene works best with JavaScript enabled. Please follow
these instructions
to activate JavaScript in your web browser.