A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders. (Q51904642)
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scientific article published in November 2010
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders. |
scientific article published in November 2010 |
Statements
A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders (English)
K M Boycott
E G Puffenberger
D Redl
A E Chudley
C Beaulieu
R Perrier
T Gillan
A Wade
J S Parboosingh
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