Ravenscroft et al., 2013 - Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy. American journal of human genetics   93(1):6-18 Full text @ Am. J. Hum. Genet.
Morpholino List (3 Records)
Target Reagent
klhl40a MO1-klhl40a
klhl40b MO1-klhl40b
MO2-klhl40b
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