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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