neurosteroid

  1. Hoopoe

    Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 .. severe fatigue, 2023, Oakley et

    Now published, see post #9. Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 as a possible cause of unexplained severe fatigue Abstract Background Causative genetic variants cannot yet be found for many disorders with a clear...
    • Hoopoe
    • Thread
    • differential diagnosis genetic genetic disorder genomics neurosteroid progesterone structural variant
    • Replies: 18
    • Forum: ME/CFS research
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