(Q48484051)

11 February 2018

title

A novel splicing mutation in the ceruloplasmin gene responsible for hereditary ceruloplasmin deficiency with hemosiderosis. (English)

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11 February 2018

author name string

Yazaki M

1

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11 February 2018

Yoshida K

2

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11 February 2018

Nakamura A

3

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11 February 2018

Furihata K

4

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11 February 2018

Yonekawa M

5

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11 February 2018

Okabe T

6

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11 February 2018

Yamashita N

7

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11 February 2018

Ohta M

8

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11 February 2018

Ikeda S

9

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11 February 2018

publication date

1 January 1998

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11 February 2018

Journal of the Neurological Sciences

number of pages

5

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based on heuristic

inferred from page(s)

published in

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11 February 2018

volume

156

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11 February 2018

issue

1

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11 February 2018

page(s)

30-34

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11 February 2018

Fine structure of the human ceruloplasmin gene

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900015-X

A nonsense mutation of the ceruloplasmin gene in hereditary ceruloplasmin deficiency with diabetes mellitus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900015-X

Aceruloplasminemia: molecular characterization of this disorder of iron metabolism

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900015-X

Complete cDNA sequence of human preceruloplasmin

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900015-X

Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900015-X

Increased plasma lipid peroxidation in patients with aceruloplasminemia

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900015-X

Use of desferrioxamine in the treatment of aceruloplasminemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900015-X

Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900015-X

Internal triplication in the structure of human ceruloplasmin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900015-X

Single-chain structure of human ceruloplasmin: the complete amino acid sequence of the whole molecule

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900015-X

Characterization of a nonsense mutation in the ceruloplasmin gene resulting in diabetes and neurodegenerative disease.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900015-X

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900015-X

10.1016/S0022-510X(98)00015-X

7 January 2021

Identifiers

DOI

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11 February 2018

1 reference

11 February 2018