QuickView for MEIS1;jsessionid=2BE570853BD2EBF9C5C28FD1B5FD7728;jsessionid=6CCF0BCA79C087D8D4558E30B1406C84;jsessionid=36C2EFAF60F43AD2E57D7B0E4E8F04C1;jsessionid=00668FA9869DFA2EBB98F85C287AC082 (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=2BE570853BD2EBF9C5C28FD1B5FD7728;jsessionid=6CCF0BCA79C087D8D4558E30B1406C84;jsessionid=36C2EFAF60F43AD2E57D7B0E4E8F04C1;jsessionid=00668FA9869DFA2EBB98F85C287AC082