(Q35076907)

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Hereditary ferritinopathy

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Europe PubMed Central

PubMed publication ID

6 August 2017

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Europe PubMed Central

title

Hereditary ferritinopathy (English)

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Europe PubMed Central

PubMed publication ID

12614943

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6 August 2017

author

Marie Bernadette Delisle

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2

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Marie Bernadette Delisle

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Olivier Rascol

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3

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Olivier Rascol

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6 August 2017

4

Bernardino Ghetti

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6 August 2017

Ruben Vidal

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12614943

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6 August 2017

publication date

1 March 2003

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12614943

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6 August 2017

published in

Journal of the Neurological Sciences

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12614943

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6 August 2017

volume

207

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12614943

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6 August 2017

issue

1-2

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12614943

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6 August 2017

page(s)

110-111

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PubMed publication ID

12614943

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6 August 2017

cites work

Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease

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https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900435-5

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7 January 2021

The role of iron in neurodegeneration: prospects for pharmacotherapy of Parkinson's disease

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https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900435-5

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7 January 2021

Identifiers

DOI

10.1016/S0022-510X(02)00435-5

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Europe PubMed Central

PubMed publication ID

12614943

retrieved

6 August 2017

PubMed publication ID

12614943

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12614943

retrieved

6 August 2017

(Q35076907)

Hereditary ferritinopathy

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