Wikidata

(Q40930062)

English

A common PEX1 frameshift mutation in patients with disorders of peroxisome biogenesis correlates with the severe Zellweger syndrome phenotype

scientific article published on July 1999

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Statements

title
A common PEX1 frameshift mutation in patients with disorders of peroxisome biogenesis correlates with the severe Zellweger syndrome phenotype (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10480353
retrieved
24 September 2017
publication date
1 July 1999
1 reference
stated in
Europe PubMed Central
PubMed ID
10480353
retrieved
24 September 2017
issue
1-2
1 reference
stated in
Europe PubMed Central
PubMed ID
10480353
retrieved
24 September 2017
page(s)
38-44
1 reference
stated in
Europe PubMed Central
PubMed ID
10480353
retrieved
24 September 2017

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                    Retrieved from "https://www.wikidata.org/w/index.php?title=Q40930062&oldid=1910851081"