QuickView for MEIS1;jsessionid=BC7297A5CD55A4C4AD690A8449D0A23B;jsessionid=82817252FB1CE431376D638F8959A1D0;jsessionid=D350B99A8521E41D8B0A11640CA0DDCD;jsessionid=619ADD0E7953464172B87874E5D5345C (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=BC7297A5CD55A4C4AD690A8449D0A23B;jsessionid=82817252FB1CE431376D638F8959A1D0;jsessionid=D350B99A8521E41D8B0A11640CA0DDCD;jsessionid=619ADD0E7953464172B87874E5D5345C