Frank Lehmann‐Horn

Researcher Next ID · RN-032259

Researcher · Biochemistry, Genetics and Molecular Biology

Ulm, Germany

Accepting doctoral researchersFunding unknown

Research interests

Biochemistry, Genetics and Molecular Biology

Medicine

Neuroscience

Ion channel regulation and function

Cardiac electrophysiology and arrhythmias

Genetic Neurodegenerative Diseases

Metabolism and Genetic Disorders

Neuroscience and Neuropharmacology Research

Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes
Nature Genetics · 2014 · https://doi.org/10.1038/ng.3130
Leitlinien für Diagnostik und Therapie in der Neurologie
Journal · 2012 · https://doi.org/10.1055/b-002-37755
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak
Journal of Clinical Investigation · 2008 · https://doi.org/10.1172/jci34438
Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current
Proceedings of the National Academy of Sciences · 2000 · https://doi.org/10.1073/pnas.97.17.9549
Genetics and pathogenesis of malignant hyperthermia
Muscle & Nerve · 2000 · https://doi.org/10.1002/(sici)1097-4598(200001)23:1<4::aid-mus3>3.0.co;2-d
Voltage-Gated Ion Channels and Hereditary Disease
Physiological Reviews · 1999 · https://doi.org/10.1152/physrev.1999.79.4.1317

No projects listed.