Publication | Closed Access
Identification of two novel mutations in OCTN2 of three patients with systemic carnitine deficiency
66
Citations
20
References
1999
Year
GeneticsInherited Metabolic DiseaseNovel MutationsPathologySystemic Carnitine DeficiencyMedicineMolecular Medicine
| Year | Citations | |
|---|---|---|
Page 1
Page 1