Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 as a possible cause of severe chronic fatigue
Oakley, Julia, Hill, Martin, Giess, Adam, Tanguy, Mélanie, Elgar, Greg
Published in Journal of translational medicine (17.11.2023)
Published in Journal of translational medicine (17.11.2023)
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