Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency - Concepedia

Concepedia

Publication | Closed Access

Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency

66

Citations

23

References

2002

Year

Stephen D. Cederbaum, Samantha Koo-McCoy, Ingrid Tein, Betty Y.L. Hsu, Arupa Ganguly, Éric Vilain, Katrina M. Dipple, Ljerka Cvitanović-Šojat, Charles A. Stanley

Molecular Genetics and Metabolism

Inherited Metabolic DiseasePhysiologyPrimary Carnitine DeficiencyMembrane BiologyLong-term FollowMedicineOctn2 Mutation

References

	Year	Citations

Page 1