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Galloway-Mowat Syndrome 9
A Galloway-Mowat syndrome characterized by onset of nephrotic syndrome with proteinuria in infancy or early childhood that is caused by homozygous mutation in the GON7 gene on chromosome 14q32.
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Overview
A Galloway-Mowat syndrome characterized by onset of nephrotic syndrome with proteinuria in infancy or early childhood that is caused by homozygous mutation in the GON7 gene on chromosome 14q32.
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