QuickView for MEIS1;jsessionid=DE4E0C148F45692259CEDA63456D514B;jsessionid=6A424B9CBD7D3AFBE025322BA95C9057;jsessionid=7A01472C2B2B4F095D5976AC2E42213B (gene)

1. A patient-enriched MEIS1 coding variant causes a restless legs syndrome-like phenotype in mice.
2. Low-grade undifferentiated sarcoma with MEIS1::NCOA2-rearrangement primary to the lung: a case repor…
3. Elucidating the importance and regulation of key enhancers for human MEIS1 expression.
4. Congenital thrombocytopenia associated with a heterozygous variant in the MEIS1 gene encoding a tran…
5. Intronic elements associated with insomnia and restless legs syndrome exhibit cell-type-specific epi…

There were no clinical trials for MEIS1;jsessionid=DE4E0C148F45692259CEDA63456D514B;jsessionid=6A424B9CBD7D3AFBE025322BA95C9057;jsessionid=7A01472C2B2B4F095D5976AC2E42213B