Condition: BARDET-BIEDL SYNDROME 5
rs121908581 in
BBS5 gene and
BARDET-BIEDL SYNDROME 5
PMID 21344540 2011 BBS genotype-phenotype assessment of a multiethnic patient cohort calls for a revision of the disease definition.
PMID 18203199 2008 Novel mutations in BBS5 highlight the importance of this gene in non-Caucasian Bardet-Biedl syndrome patients.
PMID 15137946 2004 Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene.