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

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

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