|
🐜
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The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein
15 auth.
C. Pusch,
C. Zeitz,
O. Brandau,
K. Pesch,
H. Achatz,
S. Feil,
C. Scharfe,
J. Maurer,
F. Jacobi,
A. Pinckers,
...
S. Andreasson,
A. Hardcastle,
B. Wissinger,
W. Berger,
A. Meindl
|
8 |
2000 |
8
🐜
|
|
🦁
|
Isolation of the mouse nyctalopin gene nyx and expression studies in mouse and rat retina.
8 auth.
K. Pesch,
C. Zeitz,
Julia E. Fries,
S. Münscher,
C. Pusch,
K. Kohler,
...
W. Berger,
B. Wissinger
|
4 |
2003 |
4
🦁
|
|
🐜
|
Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1
7 auth.
F. Jacobi,
M. Broghammer,
K. Pesch,
E. Zrenner,
W. Berger,
A. Meindl,
...
C. Pusch
|
3 |
2000 |
3
🐜
|
|
🐜
|
Complete form of X-linked congenital stationary night blindness: refined mapping and evidence of genetic homogeneity.
12 auth.
C. Pusch,
J. Maurer,
J. Ramser,
J. Tomiuk,
H. Achatz,
K. Pesch,
...
P. Lichtner,
E. Apfelstedt‐Sylla,
F. Jacobi,
W. Berger,
A. Meindl,
B. Wissinger
|
2 |
2001 |
2
🐜
|
|
🦁
|
Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disorders.
8 auth.
K. Pesch,
J. Tomiuk,
M. Broghammer,
E. Zrenner,
E. Apfelstedt‐Sylla,
F. Jacobi,
...
B. Wissinger,
C. Pusch
|
0 |
2001 |
0
🦁
|
