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    Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population by Billingsley, Gail (Author) , Bin, Jenea (Author) , Fieggen, Karen J. (Author) , Duncan, Jacque L. (Author) , Gerth, Christina (Author) , Ogata, Koji (Author) , Wodak, Shoshana S. (Author) , Traboulsi, Elias I. (Author) , Fishman, Gerald A. (Author) , Paterson, Andrew (Author) , Chitayat, David (Author) , Knüppel, Tanja (Author) , Millán, José M. (Author) , Mitchell, Grant A. (Author) , Deveault, Catherine (Author) , Héon, Elise (Author) ,


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