QuickView for KLHL31;jsessionid=79CFFF92B016C0CAE068FE660EAC532A (gene)

1. Epigenetics of Muscle- and Brain-Specific Expression of KLHL Family Genes.
2. Deficiency in Kelch protein Klhl31 causes congenital myopathy in mice.
3. Klhl31 attenuates β-catenin dependent Wnt signaling and regulates embryo myogenesis.
4. A Novel Intergenic Region Between KLHL31 and LRRC1-ALK Exon 20 Fusion Variant in Advanced Lung Adeno…
5. Kelch-like protein 11 antibody-associated paraneoplastic neurological syndrome: A state-of-the-art r…

There were no clinical trials for KLHL31;jsessionid=79CFFF92B016C0CAE068FE660EAC532A