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Protocol to request

CRISPR/Cas9-mediated deletion of Ephx1 in 3T3-L1 pre-adipocytes

Research article

EPHX1 mutations cause a lipoatrophic diabetes syndrome due to impaired epoxide hydrolysis and increased cellular senescence
Jeremie Gautheron et al.

DOI: 10.7554/eLife.68445

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