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on accelerating therapy development for leukodystrophies: rare genetic disorders affecting the brain's white matter. The network aims to strengthen the full translational pathway, from understanding disease
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two complementary backgrounds. You may have experience in iPSC-based disease modelling, stem-cell or cell biology and an interest in developing your data-analysis skills, or a background in
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focused on accelerating therapy development for leukodystrophies: rare genetic disorders affecting the brain's white matter. The network aims to strengthen the full translational pathway from disease
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