Natural history of multiple sulfatase deficiency: Retrospective phenotyping and functional variant analysis to characterize an ultra‐rare disease
Laura Adang(Children's Hospital of Philadelphia), Rebecca C. Ahrens‐Nicklas(Children's Hospital of Philadelphia), K. Harzer(University of Tübingen), Ida Vanessa Döederlein Schwartz(Services Hospital), Mauricio De Castro(Keesler Medical Center), Esperanza Font–Montgomery(National Human Genome Research Institute), Orna Staretz‐Chacham(Soroka Medical Center), Samuel Groeschel(University of Tübingen), Thiago Oliveira Silva(Universidade Federal do Rio Grande do Sul), Lars Schlotawa(University of Göttingen), Jutta Gärtner(German Center for Pediatric and Adolescent Rheumatology), Christiane Kehrer(University Children's Hospital Tübingen), Thomas Dierks(Bielefeld University), Carrie Costin(Akron Children's Hospital), Karthikeyan Radhakrishnan(Bielefeld University)
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