Fibrinogen Act chain mutation (Arg554 Leu) associated with hereditary renal amyloidosis in a French family (Q58260471)

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11 November 2019

title

Fibrinogen A alpha chain mutation (Arg554 Leu) associated with hereditary renal amyloidosis in a French family (English)

1 reference

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11 November 2019

author name string

L Hamidi Asl

1

1 reference

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11 November 2019

V Fournier

2

1 reference

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11 November 2019

C Billerey

3

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11 November 2019

E Justrabo

4

1 reference

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11 November 2019

D Chevet

5

1 reference

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11 November 2019

D Droz

6

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11 November 2019

C Pécheux

7

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11 November 2019

M Delpech

8

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11 November 2019

G Grateau

9

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11 November 2019

publication date

1 December 1998

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11 November 2019

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11 November 2019

volume

5

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11 November 2019

issue

4

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11 November 2019

page(s)

279-284

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Variant apolipoprotein AI as a major constituent of a human hereditary amyloid

11 November 2019

cites work

1 reference

https://api.crossref.org/works/10.3109%2F13506129809007301

Human lysozyme gene mutations cause hereditary systemic amyloidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506129809007301

Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506129809007301

Hereditary renal amyloidosis with a novel variant fibrinogen.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506129809007301

Molecular basis for fibrinogen Dusart (A alpha 554 Arg-->Cys) and its association with abnormal fibrin polymerization and thrombophilia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506129809007301

10.3109/13506129809007301

21 January 2018

Identifiers

DOI

1 reference

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11 November 2019

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