Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: A potentially lethal disorder with a new mutation

GÜNEŞ S., AYGÜN F., ÇAKAR N. E., GÜNEŞ D., BALCI M. C., YEŞİL G., ...More

Annual Symposium of the Society for the Study of Inborn Errors of Metabolism 2018, Greece, 4 September - 07 April 2018, (Summary Text)

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