(Q73143497)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10545942%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

title

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis Consortium (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10545942%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

author name string

A T Merryweather-Clarke

1

1 reference

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1 November 2019

J J Pointon

2

1 reference

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1 November 2019

J D Shearman

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10545942%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

K J Robson

4

1 reference

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1 November 2019

A M Jouanolle

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10545942%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

A Mosser

6

1 reference

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1 November 2019

V David

7

1 reference

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1 November 2019

J Y Le Gall

8

1 reference

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1 November 2019

D J Halsall

9

1 reference

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1 November 2019

T S Elsey

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10545942%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

A Kelly

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10545942%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

T M Cox

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10545942%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

M Clare

13

1 reference

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1 November 2019

A Bomford

14

1 reference

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1 November 2019

J L Vandwalle

15

1 reference

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1 November 2019

J Rochette

16

1 reference

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1 November 2019

N Borot

17

1 reference

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1 November 2019

H Coppin

18

1 reference

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1 November 2019

M P Roth

19

1 reference

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1 November 2019

E Ryan

20

1 reference

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1 November 2019

J Crowe

21

1 reference

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1 November 2019

A Totaro

22

1 reference

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1 November 2019

P Gasparini

23

1 reference

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1 November 2019

A Roetto

24

1 reference

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1 November 2019

A P Walker

25

1 reference

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1 November 2019

publication date

1 November 1999

1 reference

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1 November 2019

1 reference

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1 November 2019

volume

23

1 reference

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1 November 2019

issue

3

1 reference

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1 November 2019

page(s)

271

1 reference

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https://scigraph.springernature.com/pub.10.1038/15452

1 November 2019

exact match

0 references

cites work

Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis

1 reference

7 January 2021

An HFE intronic variant promotes misdiagnosis of hereditary hemochromatosis

1 reference

7 January 2021

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

1 reference

7 January 2021

Hereditary hemochromatosis: aHpal polymorphism within the HLA-H gene

1 reference

7 January 2021

Heterogeneity of hemochromatosis in Italy

1 reference

7 January 2021

Global prevalence of putative haemochromatosis mutations

1 reference

7 January 2021

The effect of HFE mutations on serum ferritin and transferrin saturation in the Jersey population

1 reference

7 January 2021

Rapid detection of genetic mutations associated with haemochromatosis

1 reference

7 January 2021

Haemochromatosis and HLA-H

1 reference

7 January 2021

Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients

1 reference

7 January 2021

Rapid genetic screening for haemochromatosis using heteroduplex technology

1 reference

7 January 2021

A simple genetic test identifies 90% of UK patients with haemochromatosis. The UK Haemochromatosis Consortium

1 reference

7 January 2021

Hemochromatosis in Ireland and HFE

1 reference

7 January 2021

A retrospective anonymous pilot study in screening newborns for HFE mutations in Scandinavian populations

1 reference

7 January 2021

Multicentric origin of hemochromatosis gene (HFE) mutations

1 reference

7 January 2021

A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote

1 reference

7 January 2021

Identifiers

DOI

10.1038/15452

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10545942%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1 reference