A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders

✍ Scribed by AM Innes; KM Boycott; EG Puffenberger; D Redl; IM MacDonald; AE Chudley; C Beaulieu; R Perrier; T Gillan; A Wade; JS Parboosingh

• Book ID: 110889087
• Publisher: John Wiley and Sons
• Year: 2010
• Tongue: English
• Weight: 802 KB
• Volume: 78
• Category: Article
• ISSN: 0009-9163
• DOI: 10.1111/j.1399-0004.2010.01481.x