Published in
Wiley, Journal of Inherited Metabolic Disease, 6(43), p. 1298-1309, 2020
DOI: 10.1002/jimd.12298
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Natural history of multiple sulfatase deficiency: retrospective phenotyping and functional variant analysis to characterize an ultra‐rare disease
Journal article published in 2020 by
Laura A. Adang 
,
Lars Schlotawa ,
Samuel Groeschel,
Christiane Kehrer,
Klaus Harzer,
Orna Staretz‐Chacham,
Thiago Oliveira Silva,
Ida Vanessa D. Schwartz ,
Jutta Gärtner,
Mauricio De Castro,
Carrie Costin,
Esperanza Font Montgomery,
Thomas Dierks,
Karthikeyan Radhakrishnan,
Rebecca C. Ahrens‐Nicklas
,
Lars Schlotawa ,
Samuel Groeschel,
Christiane Kehrer,
Klaus Harzer,
Orna Staretz‐Chacham,
Thiago Oliveira Silva,
Ida Vanessa D. Schwartz ,
Jutta Gärtner,
Mauricio De Castro,
Carrie Costin,
Esperanza Font Montgomery,
Thomas Dierks,
Karthikeyan Radhakrishnan,
Rebecca C. Ahrens‐Nicklas
This paper is made freely available by the publisher.
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