Search

Author/Creator Stuhlmann, Till

1. Exome sequencing reveals new causal mutations in children with epileptic encephalopathies. Issue 7 (3rd May 2013)

Authors:
Veeramah, Krishna R.; Johnstone, Laurel; Karafet, Tatiana M.; Wolf, Daniel; Sprissler, Ryan; Salogiannis, John; Barth‐Maron, Asa; Greenberg, Michael E.; Stuhlmann, Till; Weinert, Stefanie; Jentsch, Thomas J.; Pazzi, Marjorie; Restifo, Linda L.; Talwar, Dinesh; Erickson, Robert P.; Hammer, Michael F.
Journal:
Epilepsia
Issue:
Volume 54:Issue 7(2013:Jul.)
Page Start:
1270
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Uncoupling endosomal CLC chloride/proton exchange causes severe neurodegeneration. (2nd March 2020)

Authors:
Weinert, Stefanie; Gimber, Niclas; Deuschel, Dorothea; Stuhlmann, Till; Puchkov, Dmytro; Farsi, Zohreh; Ludwig, Carmen F; Novarino, Gaia; López‐Cayuqueo, Karen I; Planells‐Cases, Rosa; Jentsch, Thomas J
Journal:
EMBO journal
Issue:
Volume 39:Number 9(2020)
Page Start:
n/a
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

Limit your search