The ciliary protein Rpgrip1l in development and disease.
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DOI: 10.1016/j.ydbio.2018.07.024
Abstract: RPGRIP1L is an evolutionary highly conserved gene encoding a protein that localises at the transition zone of primary cilia. Mutations in RPGRIP1L result in ciliopathies, severe human diseases caused by dysfunctional cilia. Patients with mutations… read more here.
Keywords: rpgrip1l development; development disease; protein rpgrip1l; ciliary protein ... See more keywords