Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy (Q28139598)

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scientific article (publication date: 2000)

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Language	Label	Description	Also known as
English	Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy	scientific article (publication date: 2000)

Statements

instance of

scholarly article

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title

Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy (English)

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main subject

familial partial lipodystrophy

1 reference

based on heuristic

inferred from title

author

Robert A. Hegele

series ordinal

2

object named as

R A Hegele

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author name string

H Cao

series ordinal

1

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language of work or name

English

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publication date

1 January 2000

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published in

Human Molecular Genetics

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volume

9

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issue

1

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page(s)

109-12

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Identifiers

DOI

10.1093/HMG/9.1.109

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2738168

OpenCitations bibliographic resource ID

2738168

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2738168

PubMed publication ID

10587585

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2738168

ResearchGate publication ID

31304444

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