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Description
Two novel missense mutations of the OCTN2 gene (W283R and V446F) in a patient with primary systemic carnitine deficiency
Although attempts to disrupt dimerization via the central DD led to protein instability and hence could not test its biological significance 32 , we include both N-terminal and central DDs in our model for how PGLs mediate assembly into P granules (Fig

& Sarna, S

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