QuickView for MEIS1;jsessionid=9F1BF395348C72FFB30E42D9C13E58F9;jsessionid=135152F63BAED98E66A255646F3DE833 (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=9F1BF395348C72FFB30E42D9C13E58F9;jsessionid=135152F63BAED98E66A255646F3DE833