QuickView for MEIS1;jsessionid=2BE570853BD2EBF9C5C28FD1B5FD7728;jsessionid=6CCF0BCA79C087D8D4558E30B1406C84;jsessionid=FCA324EAE4ED4200FA3233F84003D16C;jsessionid=ABA88820E305D0327D8EF36D4797F5DA;jsessionid=C75D7FB3122BBFAACD82852E89657F2E (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=FCA324EAE4ED4200FA3233F84003D16C;jsessionid=ABA88820E305D0327D8EF36D4797F5DA;jsessionid=C75D7FB3122BBFAACD82852E89657F2E