Results
|
1.
|
|
|
2.
|
|
|
3.
|
|
|
4.
|
|
|
5.
|
|
|
6.
|
|
|
7.
|
|
|
8.
|
|
|
9.
|
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome. [electronic resource] by
- Bassuk, Alexander G
- Wallace, Robyn H
- Buhr, Aimee
- Buller, Andrew R
- Afawi, Zaid
- Shimojo, Masahito
- Miyata, Shingo
- Chen, Shan
- Gonzalez-Alegre, Pedro
- Griesbach, Hilary L
- Wu, Shu
- Nashelsky, Marcus
- Vladar, Eszter K
- Antic, Dragana
- Ferguson, Polly J
- Cirak, Sebahattin
- Voit, Thomas
- Scott, Matthew P
- Axelrod, Jeffrey D
- Gurnett, Christina
- Daoud, Azhar S
- Kivity, Sara
- Neufeld, Miriam Y
- Mazarib, Aziz
- Straussberg, Rachel
- Walid, Simri
- Korczyn, Amos D
- Slusarski, Diane C
- Berkovic, Samuel F
- El-Shanti, Hatem I
Producer: 20090106
In:
American journal of human genetics vol. 83
Availability: No items available.
|