Mutational Analysis of SDCCAG8 in Bardet-Biedl Syndrome Patients with Renal Involvement and Absent Polydactyly

Title
Mutational Analysis of SDCCAG8 in Bardet-Biedl Syndrome Patients with Renal Involvement and Absent Polydactyly
Authors
Keywords
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Journal
OPHTHALMIC GENETICS
Volume 33, Issue 3, Pages 150-154
Publisher
Informa UK Limited
Online
2012-05-25
DOI
10.3109/13816810.2012.689411

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