Acid ceramidase deficiency due to mutations in ASAH1, presenting asFarber Disease: Diagnostic data from the first-ever natural history study

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solyom A., Ferreira C. R., Mitchell J., Guelbert N., ÖNENLİ MUNGAN H. N., BULUT F. D., ...More

American Society of Human Genetics 69th Annual Meeting, 2019, Houston, United States Of America, 15 - 19 September 2019, (Summary Text)

• Publication Type: Conference Paper / Summary Text
• City: Houston
• Country: United States Of America
• Çukurova University Affiliated: Yes