<i>MYO1E</i>Mutations and Childhood Familial Focal Segmental Glomerulosclerosis
Article 2011 en
Authors
CM
Caterina Mele
PI
Paraskevas Iatropoulos
RD
Roberta Donadelli
Abstract
1 min read
MYO1E mutations are associated with childhood-onset, glucocorticoid-resistant focal segmental glomerulosclerosis. Our data provide evidence of a role of Myo1E in podocyte function and the consequent integrity of the glomerular filtration barrier.
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