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Published in 2018 at "Oncotarget"
DOI: 10.18632/oncotarget.25259
Abstract: Ciliopathies are a group of genetically heterogeneous disorders, characterized by defects in cilia genesis or maintenance. Mutations in the RPGR gene and its interacting partners, RPGRIP1 and RPGRIP1L, cause ciliopathies, but the function of their…
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Keywords:
rpgrip1 rpgrip1l;
activity;
rpgrip1l;
rpgr rpgrip1 ... See more keywords