Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly (Q35546499)
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scientific article published on 14 September 2011
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly |
scientific article published on 14 September 2011 |
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Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly (English)
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A Toutain
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E Schaefer
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A Zaloszyc
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J Lauer
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M Durand
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F Stutzmann
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Y Perdomo-Trujillo
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C Redin
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V Bennouna Greene
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L Perrin
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M Gérard
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S Caillard
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R A Lewis
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D Christmann
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J Letsch
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M Kribs
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C Mutter
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C Stoetzel
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M Fischbach
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V Marion
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H Dollfus
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14 September 2011
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6
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273-281
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Identifiers
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