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human TTC8 protein

homozygous null BBS8 mutation leads to Bardet-Biedl syndrome with randomization of left-right body axis symmetry, a known defect of the nodal cilium; RefSeq NM_144596
Also Known As:
TTC8 protein, human; BBS8 protein, human; Bardet- Biedl syndrome 8 protein, human; TPR repeat protein 8, human; tetratricopeptide repeat domain 8 protein, human
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Bio-Agent Context: Research Results