The development of atypical hemolytic uremic syndrome depends on complement C5 (Q28300378)

1

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Marina Botto

7

object named as

Marina Botto

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Paolo Macor

object named as

Paolo Macor

2

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Matthew C Pickering

object named as

Matthew C Pickering

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author name string

Danielle Paixão-Cavalcante

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Kirsten L Rose

4

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Franco Tedesco

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H Terence Cook

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Marina Botto

Journal of the American Society of Nephrology

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language of work or name

English

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publication date

January 2011

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published in

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volume

22

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issue

1

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page(s)

137-45

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cites work

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Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome

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Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndrome

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