OCTN2 Gene Mutations in Turkish Patients with Primary Carnitine Deficiency

YÜCEL YILMAZ D., ERSOY M., CANDAN Ş., BALCI M. C., KILIÇ M., GÖKÇAY G. F., ...More

2012 Annual Symposium of the Society for the Study of Inborn Errors of Metabolism-United Kingdom, 4 - 07 September 2012, (Summary Text)

• Publication Type: Conference Paper / Summary Text
• Istanbul University Affiliated: Yes