SLC22A5 mutants [plasma membrane]

Stable Identifier
R-HSA-5625715
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
plasma membrane
Locations in the PathwayBrowser
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Participants
members
Disease
Name Identifier Synonyms
systemic primary carnitine deficiency disease DOID:14365 carnitine uptake defect, carnitine transporter deficiency, primary carnitine deficiency, deficiency of plasma-membrane carnitine transporter, renal carnitine transport defect (disorder)
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