Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly

Publisher： Karger

E-ISSN： 1661-8777|1|6|273-281

ISSN： 1661-8769

Source： Molecular Syndromology, Vol.1, Iss.6, 2011-09, pp. : 273-281

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