(Q33460351)

27 July 2017

Recurrent hemolytic-uremic syndrome with the hypomorphic fast allele of the third component of complement (English)

1 reference

hemolytic-uremic syndrome

27 July 2017

1 reference

Wyatt RJ

1

1 reference

27 July 2017

Jones D

2

1 reference

27 July 2017

Stapleton FB

3

1 reference

27 July 2017

Roy S 3rd

4

1 reference

27 July 2017

Odom TW

5

1 reference

27 July 2017

McLean RH

6

1 reference

27 July 2017

language of work or name

English

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publication date

1 October 1985

1 reference

The Journal of Pediatrics

27 July 2017

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27 July 2017

107

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27 July 2017

4

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27 July 2017

564-566

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Partial lipodystrophy and familial C3 deficiency

27 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980022-6

An inherited defect in the C3 convertase, C3b,Bb, associated with glomerulonephritis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980022-6

Hypomorphic variant of the slow allele of C3 associated with hypocomplementemia and hematuria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980022-6

Studies of a hypomorphic variant of human C3

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980022-6

Familial partial deficiency of the third component of complement (C3) and the hypocomplementemic cutaneous vasculitis syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980022-6

Genetically determined variation in the complement system: relationship to disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980022-6

10.1016/S0022-3476(85)80022-6

7 January 2021

Identifiers

DOI

1 reference

27 July 2017

1 reference