Advances in Hepatology
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چکیده
SG The more common form of PLD is an extrarenal manifestation of autosomal dominant polycystic kidney disease. The less common form of isolated PLD is an autosomal dominant inherited condition and has been associated with 2 distinct mutations: the PRKCSH gene that encodes for hepatocystin and the SEC63 gene that encodes for a component of the protein translocation machinery in the endoplasmic reticulum.
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تاریخ انتشار 2013