(Q43834889)

27 November 2017

title

Rapid detection of the Wilson's disease H1069Q mutation by melting curve analysis with the LightCycler (English)

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27 November 2017

H Witt

1

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27 November 2017

O Landt

series ordinal

2

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27 November 2017

publication date

1 October 2001

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Clinical Chemistry and Laboratory Medicine

27 November 2017

published in

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27 November 2017

volume

39

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27 November 2017

issue

10

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27 November 2017

page(s)

953-955

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The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene

27 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.153

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.153

The Wilson disease gene: spectrum of mutations and their consequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.153

Efficient detection of mutations in Wilson disease by manifold sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.153

Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.153

Wilson's disease in patients presenting with liver disease: a diagnostic challenge.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.153

Wilson disease: genetic basis of copper toxicity and natural history

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.153

21 January 2018

Identifiers

DOI

10.1515/CCLM.2001.153

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27 November 2017

1 reference