A founder mutation in BBS2 is responsible for Bardet-Biedl...

Clinical Genetics 2010 Vol. 78; Iss. 5

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

AM Innes, KM Boycott, EG Puffenberger, D Redl, IM MacDonald, AE Chudley, C Beaulieu, R Perrier, T Gillan, A Wade, JS Parboosingh
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Volume:
78
Year:
2010
Language:
english
Pages:
8
DOI:
10.1111/j.1399-0004.2010.01481.x
File:
PDF, 802 KB
english, 2010
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