(Q43795706)

26 November 2017

title

A spontaneous novel XK gene mutation in a patient with McLeod syndrome (English)

1 reference

26 November 2017

Supple SG

1

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26 November 2017

Iland HJ

series ordinal

2

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26 November 2017

Barnett MH

series ordinal

3

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26 November 2017

Pollard JD

series ordinal

4

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26 November 2017

language of work or name

English

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publication date

1 November 2001

1 reference

British Journal of Haematology

26 November 2017

published in

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26 November 2017

volume

115

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26 November 2017

issue

2

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26 November 2017

page(s)

369-372

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Unusual muscle pathology in McLeod syndrome

26 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.03121.X

The 1993-94 Généthon human genetic linkage map

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.03121.X

A novel frameshift mutation in the McLeod syndrome gene in a Japanese family

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.03121.X

Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.03121.X

McLeod syndrome: a novel mutation, predominant psychiatric manifestations, and distinct striatal imaging findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.03121.X

Purification and partial characterization of the erythrocyte Kx protein deficient in McLeod patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.03121.X

Association of XK and Kell blood group proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.03121.X

10.1046/J.1365-2141.2001.03121.X

21 January 2018

Identifiers

DOI

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26 November 2017

1 reference