solyom, A. Et Al. 2019. Acid ceramidase deficiency due to mutations in ASAH1, presenting asFarber Disease: Diagnostic data from the first-ever natural history study. American Society of Human Genetics 69th Annual Meeting, 2019 , (Houston, United States Of America).

solyom, A., Ferreira, C. R., Mitchell, J., Guelbert, N., ÖNENLİ MUNGAN, H. N., BULUT, F. D., ... Magnusson, B.(2019). Acid ceramidase deficiency due to mutations in ASAH1, presenting asFarber Disease: Diagnostic data from the first-ever natural history study . American Society of Human Genetics 69th Annual Meeting, 2019, Houston, United States Of America

solyom, Alexander Et Al. "Acid ceramidase deficiency due to mutations in ASAH1, presenting asFarber Disease: Diagnostic data from the first-ever natural history study," American Society of Human Genetics 69th Annual Meeting, 2019, Houston, United States Of America, 2019

solyom, Alexander Et Al. "Acid ceramidase deficiency due to mutations in ASAH1, presenting asFarber Disease: Diagnostic data from the first-ever natural history study." American Society of Human Genetics 69th Annual Meeting, 2019 , Houston, United States Of America, 2019

solyom, A. Et Al. (2019) . "Acid ceramidase deficiency due to mutations in ASAH1, presenting asFarber Disease: Diagnostic data from the first-ever natural history study." American Society of Human Genetics 69th Annual Meeting, 2019 , Houston, United States Of America.

@conferencepaper{conferencepaper, author={Alexander solyom Et Al. }, title={Acid ceramidase deficiency due to mutations in ASAH1, presenting asFarber Disease: Diagnostic data from the first-ever natural history study}, congress name={American Society of Human Genetics 69th Annual Meeting, 2019}, city={Houston}, country={United States Of America}, year={2019}}