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Indeed, a rare case has been described of a family presenting with a particularly mild PKD manifestation, with recessive inheritance that was caused by a homozygous inheritance of a hypomorphic PKD1 mutation (p.R3277C) (4)
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Additionally, there is also no convincing evidence to show that GH influences Glut4 translocation and subsequently glucose uptake (Khalfallah et al., 2001
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