The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome.
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| Description | scientific article |
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author: Wolf Hervé Fridman Catherine Sautès-Fridman Marie-Agnès Dragon-Durey |
| Publication date | May 11, 2009 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |