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KLHL31;jsessionid=03325FB071AEC0D3235143A24965AE2E
(gene)
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Epigenetics of Muscle- and Brain-Specific Expression of KLHL Family Genes.
Deficiency in Kelch protein Klhl31 causes congenital myopathy in mice.
Klhl31 attenuates β-catenin dependent Wnt signaling and regulates embryo myogenesis.
A Novel Intergenic Region Between KLHL31 and LRRC1-ALK Exon 20 Fusion Variant in Advanced Lung Adeno…
Kelch-like protein 11 antibody-associated paraneoplastic neurological syndrome: A state-of-the-art r…
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There were no clinical trials for KLHL31;jsessionid=03325FB071AEC0D3235143A24965AE2E
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