Mutational Analysis of SDCCAG8 in Bardet-Biedl Syndrome Patients with Renal Involvement and Absent Polydactyly
Billingsley, Gail, Vincent, Ajoy, Deveault, Catherine, Héon, EliseVolume:
33
Language:
english
Journal:
Ophthalmic Genetics
DOI:
10.3109/13816810.2012.689411
Date:
September, 2012
File:
PDF, 852 KB
english, 2012