(Q52552499)

3 May 2018

title

Lamin B-receptor mutations in Pelger-Huët anomaly. (English)

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3 May 2018

author

David C. Rees

7

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3 May 2018

Swee Lay Thein

6

object named as

Swee Lay Thein

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3 May 2018

author name string

Steve Best

1

1 reference

3 May 2018

Filippo Salvati

2

1 reference

3 May 2018

Juraj Kallo

3

1 reference

3 May 2018

Chad Garner

4

1 reference

3 May 2018

Sue Height

5

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3 May 2018

language of work or name

English

0 references

publication date

1 November 2003

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3 May 2018

British Journal of Haematology

published in

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3 May 2018

volume

123

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3 May 2018

issue

3

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3 May 2018

page(s)

542-544

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3 May 2018

The human lamin B receptor/sterol reductase multigene family

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2003.04621.X

Crossref

reference URL

retrieved

21 January 2018

Autosomal recessive HEM/Greenberg skeletal dysplasia is caused by 3 beta-hydroxysterol delta 14-reductase deficiency due to mutations in the lamin B receptor gene

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2003.04621.X

Crossref

reference URL

retrieved

21 January 2018

Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huet anomaly

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2003.04621.X

Crossref

reference URL

retrieved

21 January 2018

Identifiers

DOI

10.1046/J.1365-2141.2003.04621.X

1 reference

3 May 2018

PubMed ID

14617022

1 reference

3 May 2018