Wikidata

(Q44707634)

English

Severe phenotype of chronic granulomatous disease presenting in a female with a de novo mutation in gp91-phox and a non familial, extremely skewed X chromosome inactivation

scientific article published in December 2003

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Statements

title
Severe phenotype of chronic granulomatous disease presenting in a female with a de novo mutation in gp91-phox and a non familial, extremely skewed X chromosome inactivation (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
14697745
retrieved
5 December 2017
author name string
Mindy Anderson-Cohen
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
14697745
retrieved
5 December 2017
Steve M Holland
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
14697745
retrieved
5 December 2017
Doug B Kuhns
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
14697745
retrieved
5 December 2017
Thomas A Fleisher
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
14697745
retrieved
5 December 2017
Sebastian Brenner
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
14697745
retrieved
5 December 2017
publication date
1 December 2003
1 reference
stated in
Europe PubMed Central
PubMed ID
14697745
retrieved
5 December 2017
page(s)
308-317
1 reference
stated in
Europe PubMed Central
PubMed ID
14697745
retrieved
5 December 2017

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                    Retrieved from "https://www.wikidata.org/w/index.php?title=Q44707634&oldid=2033387076"