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the decrease in HGF-dependent MDCK proliferation below control levels for some compounds is not surprising since the experiment was earned in 2% serum, which likely contains some level of HGF

Dnm2 mutations cause autosomal dominant centronuclear myopathy, a rare form of congenital myopathy, and intermediate and axonal forms of Charcot-Marie-Tooth disease, a peripheral neuropathy [51,52]

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This is often accompanied by occasional spikewave or intermittent to continuous spikewave or multi-spikewave activity, known as rhythmic high-amplitude delta with superimposed (poly)spikes (RHADS) (44)