Wikidata

(Q30009845)

English

Functional analysis of PEX13 mutation in a Zellweger syndrome spectrum patient reveals novel homooligomerization of PEX13 and its role in human peroxisome biogenesis.

scientific article published on 27 May 2013

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Statements

title
Functional analysis of PEX13 mutation in a Zellweger syndrome spectrum patient reveals novel homooligomerization of PEX13 and its role in human peroxisome biogenesis (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
23716570
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23716570%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 March 2020

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