Diagnosis of glycine encephalopathy in a pediatric patient by detection of a GLDC gene mutation by next generation DNA sequencing

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EZGÜ F. S., ÇİFTÇİ B., TOPÇU B., ADIYAMAN G., GÖKMENOĞLU H., KÜÇÜKÇONGAR A., ...More

Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Innsbruck, 2-5 September 2014, 2 - 05 September 2014

• Publication Type: Conference Paper
• Ankara Yıldırım Beyazıt University Affiliated: No