Corrigendum: Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency (Human Molecular Genetics (1999) 8 (655-660))

Human Molecular Genetics

Volumn 8, Issue 5, 1999, Pages 943-

  Tang, N L S ^a   Ganapathy, V ^a   Wu, X ^a   Hui, J ^a   Seth, P ^a   Yuen, P M P ^a   Wanders, R J A ^a   Fok, T F ^a   Hjelm, N M ^a  

^a NONE

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Indexed keywords

ERRATUM; ERROR; PRIORITY JOURNAL;

EID: 0032899974     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Erratum

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