Wirth, Brunhilde

Biallelic loss of proprioception-related PIEZO2 causes muscular atrophy with perinatal respiratory distress, arthrogryposis, and scoliosis

Delle Vedove, A., Storbeck, M., Heller, R., Hölker, I., Hebbar, M., Shukla, A., Magnusson, O., Cirak, S., Girisha, K. M., O’Driscoll, M., et al. (2016) · The American Journal of Human Genetics

Hereditary Neurological DisordersMuscle Physiology and Disorders

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Genetic modifiers ameliorate endocytic and neuromuscular defects in a model of spinal muscular atrophy

Walsh, M. B., Janzen, E., Wingrove, E., Hosseinibarkooie, S., Muela, N. R., Davidow, L., Dimitriadi, M., Norabuena, E. M., Rubin, L. L., Wirth, B., et al. (2020) · BMC Biology

Neurogenetic and Muscular Disorders ResearchAmyotrophic Lateral Sclerosis Research

Cited by 22