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UnknownDisruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy.
Not available
S-EPMC4129401 | biostudies-literature
UnknownActive transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain.
Not available
S-EPMC3854969 | biostudies-literature
UnknownAn organelle-specific protein landscape identifies novel diseases and molecular mechanisms.
Not available
S-EPMC4869170 | biostudies-literature
UnknownTCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.
Not available
S-EPMC4468853 | biostudies-literature
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