A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans (Q28287958)

2

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S Takeda

3

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A Nakamura

4

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K Yamamoto

5

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H Morita

6

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S Hiyamuta

7

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S Ikeda

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N Shimizu

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N Yanagisawa

https://scigraph.springernature.com/pub.10.1038/ng0395-267

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language of work or name

English

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publication date

March 1995

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published in

Nature Genetics

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volume

9

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issue

3

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page(s)

267-72

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exact match

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cites work

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Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein

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Isolation of a partial candidate gene for Menkes disease by positional cloning

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

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