Cite
HARVARD Citation
Bee, Y. et al. (2015). Whole Exome Sequencing Identifies a Novel and a Recurrent Mutation in BBS2 Gene in a Family with Bardet-Biedl Syndrome. BioMed research international. p. . [Online].
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Bee, Y. et al. (2015). Whole Exome Sequencing Identifies a Novel and a Recurrent Mutation in BBS2 Gene in a Family with Bardet-Biedl Syndrome. BioMed research international. p. . [Online].