Sundberg, E. Et Al. 2019. Farber disease (acid ceramidase deficiency): demographic and diagnostic data from the first-ever natural history study. 52nd Conference of the European-Society-of-Human-Genetics (ESHG) , (Gothenburg, Sweden), 1332-1333.

Sundberg, E., Magnusson, B., Ferreira, C. R., Grant, C., Mitchell, J., Harmatz, P., ... Mungan, N. O.(2019). Farber disease (acid ceramidase deficiency): demographic and diagnostic data from the first-ever natural history study . 52nd Conference of the European-Society-of-Human-Genetics (ESHG) (pp.1332-1333). Gothenburg, Sweden

Sundberg, E. Et Al. "Farber disease (acid ceramidase deficiency): demographic and diagnostic data from the first-ever natural history study," 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg, Sweden, 2019

Sundberg, E. Et Al. "Farber disease (acid ceramidase deficiency): demographic and diagnostic data from the first-ever natural history study." 52nd Conference of the European-Society-of-Human-Genetics (ESHG) , Gothenburg, Sweden, pp.1332-1333, 2019

Sundberg, E. Et Al. (2019) . "Farber disease (acid ceramidase deficiency): demographic and diagnostic data from the first-ever natural history study." 52nd Conference of the European-Society-of-Human-Genetics (ESHG) , Gothenburg, Sweden, pp.1332-1333.

@conferencepaper{conferencepaper, author={E. Sundberg Et Al. }, title={Farber disease (acid ceramidase deficiency): demographic and diagnostic data from the first-ever natural history study}, congress name={52nd Conference of the European-Society-of-Human-Genetics (ESHG)}, city={Gothenburg}, country={Sweden}, year={2019}, pages={1332-1333} }