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bardet-biedl syndrome, modifier of
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ARL6
Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3)
TMEM67
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)
CCDC28B
Dissection of epistasis in oligogenic Bardet-Biedl syndrome
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