Publications by authors named "T Stuhlmann"

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Uncoupling endosomal CLC chloride/proton exchange causes severe neurodegeneration.
Stefanie Weinert, Niclas Gimber, Dorothea Deuschel, Till Stuhlmann, Dmytro Puchkov

EMBO J· May 2020

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LRRC8/VRAC anion channels enhance β-cell glucose sensing and insulin secretion.
Till Stuhlmann, Rosa Planells-Cases, Thomas J Jentsch

Nat Commun· May 2018

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De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females.
E E Palmer, T Stuhlmann, S Weinert, E Haan, H Van Esch

Mol Psychiatry· February 2018

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X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.
H Hu, S A Haas, J Chelly, H Van Esch, M Raynaud, T Stuhlmann

Mol Psychiatry· January 2016

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Exome sequencing reveals new causal mutations in children with epileptic encephalopathies.
Krishna R Veeramah, Laurel Johnstone, Tatiana M Karafet, Daniel Wolf, Ryan Sprissler, Till Stuhlmann

Epilepsia· July 2013

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