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JMG.2008.064766
JMG.2008.064766
http://dx.doi.org/10.1136/JMG.2008.064766
The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome.
P356
Q33384470-866D23EE-4287-4143-AD4A-187780B8B5F0
P356
JMG.2008.064766
http://dx.doi.org/10.1136/JMG.2008.064766