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

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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