Wikidata

(Q46695318)

English

Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome

scientific article

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Statements

title
Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16153625
retrieved
24 December 2017
reference URL
http://europepmc.org/abstract/MED/16153625

Identifiers

 
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