(Q43791985)

26 November 2017

title

Gene-scan method for the recognition of carriers and patients with p47(phox)-deficient autosomal recessive chronic granulomatous disease (English)

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26 November 2017

Dekker J

1

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26 November 2017

de Boer M

series ordinal

2

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26 November 2017

Roos D

series ordinal

3

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26 November 2017

language of work or name

1 reference

1 November 2001

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26 November 2017

published in

Experimental Hematology

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26 November 2017

volume

29

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26 November 2017

issue

11

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26 November 2017

page(s)

1319-1325

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Autosomal recessive chronic granulomatous disease caused by deletion at a dinucleotide repeat

26 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0301-472X%2801%2900731-7

7 January 2021

In vitro molecular reconstitution of the respiratory burst in B lymphoblasts from p47-phox-deficient chronic granulomatous disease

1 reference

https://api.crossref.org/works/10.1016%2FS0301-472X%2801%2900731-7

7 January 2021

Homologous dinucleotide (GT or TG) deletion in Japanese patients with chronic granulomatous disease with p47-phox deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0301-472X%2801%2900731-7

7 January 2021

Autosomal recessive chronic granulomatous disease caused by defects in NCF-1, the gene encoding the phagocyte p47-phox: mutations not arising in the NCF-1 pseudogenes

1 reference

https://api.crossref.org/works/10.1016%2FS0301-472X%2801%2900731-7

7 January 2021

Mutational analysis of patients with p47-phox-deficient chronic granulomatous disease: The significance of recombination events between the p47-phox gene (NCF1) and its highly homologous pseudogenes

1 reference

https://api.crossref.org/works/10.1016%2FS0301-472X%2801%2900731-7

7 January 2021

A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease

1 reference

https://api.crossref.org/works/10.1016%2FS0301-472X%2801%2900731-7

7 January 2021

A complete physical contig and partial transcript map of the Williams syndrome critical region.

1 reference

https://api.crossref.org/works/10.1016%2FS0301-472X%2801%2900731-7

7 January 2021

10.1016/S0301-472X(01)00731-7

Identifiers

DOI

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26 November 2017

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