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Innes AM, Boycott KM, Puffenberger EG, Redl D, MacDonald IM, Chudley AE, Beaulieu C, Perrier R, Gillan T, Wade A, Parboosingh JS. A founder mutation in BBS2 is...
RNA | Analysis | Genomics | Genetic research | Physiological aspects | Boycotts | Genetic aspects | Ophthalmology | Bardet-Biedl syndrome | Single-nucleotide polymorphism | Mutation
RNA | Analysis | Genomics | Genetic research | Physiological aspects | Boycotts | Genetic aspects | Ophthalmology | Bardet-Biedl syndrome | Single-nucleotide polymorphism | Mutation
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